Gram-positive bacterium transformed with a replicon

ABSTRACT

A recombinant vector capable of replicating in Gram positive bacteria and containing: a) a nucleotide concatenation I of  Bacillus thuringiensis  with a size of about 2.6 kb between sites BalI-HpaI, or any fragment included in said concatenation as long as its allows replication of the recombinant vector when under the control of functional promoter in Gram positive bacteria, or any sequence which hybridizes with the complementary sequence of concatenation I or the above mentioned fragment under highly stringent conditions, and b) at least on DNA sequence of interest inserted in phase with the above mentioned concatenation.

This application is a divisional of U.S. application Ser. No. 08/955,091, filed on Oct. 21, 1997 now U.S. Pat. No. 5,928,897, which is a Divisional of U.S. application Ser. No. 08/178,242, filed May 18, 1994, now U.S. Pat. No. 5,766,586, which is a 371 of PCT/FR92/00711, filed Jul. 20 1992.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to a novel type A Gram-positive replicon and its use for the construction of recombinant vectors.

2. Discussion of the Background

The naturally occurring bacterial plasmids are usually endowed with a high degree of stability. If they are distributed randomly the theoretical probability (L) of producing a plasmid-free cell is given by the equation: L=(½)^(2n) (where n is the number of plasmid molecules per cell and it is supposed that 2n copies of the plasmid are present immediately prior to division). Thus, high copy number plasmids can be maintained in a stable manner following random distribution, whereas efficient mechanisms are necessary to prevent the loss of low copy number plasmids in the absence of selection pressure (Nordström and Austin, 1989 Annu. Rev. Genet. 23: 37-69).

In Gram-negative bacteria several systems involving maintenance functions for the plasmids have been described for low copy number plasmids such as F, P1 and R1. They comprise the hok/sok and ccd systems responsible for the post-segregational destruction of the cells which lose plasmids (Jaffé et al., 1985 J. Bacteriol. 163: 841-849; Gerdes et al., 1986 Mol. Microbiol. 4: 1807-1818) and true partition functions which ensure that each daughter cell receives a plasmid molecule (Austin and Nordström 1990 Cell 60: 351-354). Furthermore, auxiliary functions which allow random distribution of the replicons have been described. Examples include the site-specific recombination system of Col E1 (Summers and Sherrat, 1984 Cell 36: 1097-1103) and the par locus of pSC101 (Tucker et al., 1984 Cell 38: 191-201).

In Gram-positive bacteria, much less information is available concerning the functions required for the stable maintenance of the plasmids, In the plasmids with high or low copy numbers which replicate by a “rolling circle” mechanism through a single-stranded DNA intermediate (te Riele et al., 1986a EMBO J. 5: 631-637, 1986b Proc. Natl. Acad. Sci. USA 83: 2541-2545; Gruss and Ehrlich, 1989 Microbiol. Rev. 53: 231-241), the stability is coupled to replication and not to a discrete function. In the case of various known plasmids pUB110, pTA1060, pMV158 (Bron et al., 1991b Plasmid 19: 231-241), and pLS11 (Chang et al., 1987 J. Bacteriol. 169: 3952-3962), the regions of stability are the “negative” origins controlling the conversion of the single-stranded DNA into double-stranded plasmid DNA The replication of these plasmids is guaranteed by a protein encoded in the plasmid. These plasmids are frequently unstable from a structural and segregational point of view when they are used as cloning vectors, and this is probably due to their particular mode of replication.

A second class of Gram-positive replicons comprises the large plasmids with low copy numbers, pTB19, pIP404 and pAMbeta1 (Imanaka et al., 1986 Mol. Gen. Genet. 20: 90-96; Garneir and Cole, 1988 Plasmid 19: 151-160; Swinfield et al., 1990 Gene 87: 79-90). Their replication requires a protein encoded in the plasmid which does not share any homology with that of the plasmids whose replication involves a “rolling circle” mechanism. These plasmids do not accumulate single-stranded DNA during replication (Garnier and Cole, 1988 Plasmid 19: 151-160; Jannière et al., 1990 Gene 87: 53-61) and are structurally stable (Jannière et al., 1990 Gene 87: 53-61).

No information is available concerning the potential partition functions of these plasmids with low copy numbers However, these functions are essential for their maintenance in sporulating Gram-positive bacteria such as the Bacillus species During the differentiation stage of these bacteria, the spore compartment represents only about one sixth of the cell, and the probability of producing a plasmid-free spore is: L=(⅚)^(2n). A random distribution of the plasmids during sporulation may, consequently, lead to a serious loss of replicons (with n<10) in the spore population.

The sporulating Gram-positive bacterium Bacillus thuringiensis is known for its capacity to produce insecticidal toxins during sporulation (Lereclus et al., 1989b Regulation of Procaryotic Development. American Society for Microbiology, Washington D.C., 255-276). These parasporal proteins (delta-endotoxins) are each classified as being either CryI, II, III or IV as a function of their activity spectrum towards insect larvae (Höfte and Whitely, 1989 Microbiol. Rev. 53: 242-255). Different cry genes coding for delta-endotoxins active against various orders of insects have been cloned, and transformation by electroporation now makes possible the analysis of their expression in their natural host and the construction of strains obtained by genetic engineering exhibiting improved properties for insect control. B. thuringiensis exhibits a complex series of resident plasmids in most of the strains examined (Gonzalez et al., 1981 Plasmid 5: 351-365; Lereclus et al., 1982 Mol. Gen. Genet. 186: 391-398; Kronstad et al., 1983 J. Bacteriol 154: 419-428). The quite widespread presence of these plasmids suggests very efficient stability and replication functions. Starting from that observation, cloning and characterization studies of small cryptic plasmids (Mahillan et al., 1988 Plasmid 19: 169-173; Mahillon and Seurinck, 1988 Nucleic Acids Res. 16: 11827-11828; McDowell et al., 1991 Plasmid 25: 113-120) and the isolation of the replication regions of large plasmids (Baum et al., 1990 Appl. Environ. Microbiol. 56: 3420-3428) and of two smaller plasmids pHT1000 and pHT1030 of 8.6 kb and 15 kb, respectively (Leredus et al., FEMS Microbiol. Lett. 49: 417-422) have been accomplished. pHT1030 was studied on account of its high segregation stability in B. subtilis, and a 2.9 kb DNA fragment including the stability and replication function of pHT1030 was used to construct the shuttle vector pHT3101 (Lereclus et al., 1989a FEMS Microbiol. Lett. 60: 211-218; Debarbouillé et al., 1990 J. Bacteriol. 172: 3966-3973).

SUMMARY OF THE INVENTION

With the objective of defining agents specific for the construction of cloning vectors and, optimally, expression vectors suited to the transformation of bacteria and, in particular, Gram-positive bacteria, the inventors have identified within the 2.9 kb DNA fragment of the plasmid pHT1030 (Lereclus et al., 1989a FEMS Microbiol. Lett 60: 211-218) a nucleotide sequence of about 2.6 kb and, within this sequence, different specific sequences for the stability and replication functions of plasmids used to transform Gram-positive bacteria.

The identification of these specific sequences has made it possible to define more precisely those which might be the elements of the 2.6 kb fragment which can be used in the context of the construction of recombinant vectors designed for the cloning and, optionally, the expression of sequences in Gram-positive bacteria for the purpose of modulating the behaviour of the vector in its host, for example for the purpose of modulating the stability and the number of copies of such vectors in a given bacterium. In fact, the inventors have observed that the stability function carried by the 2.6 kb fragment may be a nuisance in some applications such as the preparation of a recombinant vector used to transform bacteria themselves designed to be dispersed in the environment.

The results obtained by the inventors in the context of the invention thus make it possible to envisage the construction of vectors capable of being adapted to specific uses.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1A and 1B: Nucleotide sequence of the BalI restriction fragment of pHT1030 and deduced amino acid sequences of ORF1 (FIGS. 1A and 1B) and ORF2 (FIG. 1A) (SEQ ID NOS:1-3).

FIG. 2: Construction of deletion derivatives of pHT1030 and analysis of their replication and stability in the Bacilli.

FIG. 3: Analysis of the production of single-stranded DNA in cells containing deletion derivatives of pHT1030.

FIG. 4: Expression of the spbb gene in an in vitro E. coli transcription-translation system.

FIGS. 5A-5B: Segregation stability of the deletion derivatives of pHT1030 during vegetative growth.

FIGS. 6A-6B: Segregation stability of the deletion derivatives of pHT1030 during sporulation.

FIG. 7: Construction of the pBC16 variants carrying regions of the spbB locus.

FIG. 8: Stability of the pBC16 variants bearing the spbB regions.

FIG. 9: Elimination of the HindIII site of pHT1035 and selection of variants with a high copy number.

FIG. 10: Construction of the shuttle vectors pHT304, pHT315 and pHT370.

FIG. 11: Analysis of the proteins of the B. thuringiensis transformants expressing the cryIIIA gene.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Different levels of adaptation may be envisaged in the light of the knowledge acquired by the inventors: As an example, the degree of replication of recombinant vectors constructed on the basis of the present invention in Gram-positive bacteria may be modulated.

Similarly, the segregational stability of these plasmids may be controlled by acting on certain specific parameters.

Another advantage of the invention results from the fact that the vectors used to transform Gram-negative bacteria, and particularly advantageously Gram-positive bacteria, use host proteins for their replication.

Hence, the object of the invention is a recombinant vector capable of replicating in Gram-positive bacteria, and optionally, of functioning as an expression vector in these bacteria. The invention also relates to the different nucleotide fragments which can be used in the context of the construction of vectors suited for the transformation of Gram-positive bacteria involved in the stability and/or replication functions of the vector constructed. Host cells transformed by the vectors defined above as well as compositions involving the transformants are also included in the scope of the invention.

The invention also relates to a procedure for the preparation of the vectors as well as a procedure for the transformation of the cell strains.

A recombinant vector capable of replicating in Gram-positive bacteria is characterized in that it contains:

a) a nucleotide sequence I (SEQ ID NO:4) of Bacillus thuringiensis of about 2.6 kb included between the BalI-HpaI sites and corresponding to the sequence below defined by the nucleotides 1 to 2642 or,

any fragment included in this sequence provided that it allows the replication at the recombinant vector when it is under the control of a promoter which is functional in Gram-positive bacteria or,

any sequence which hydridizes with the complementary sequence of sequence I or the above fragment under conditions of high stringency, and

b) at least one DNA sequence of interest inserted in phase with the above sequence.

A sequence hybridizing with the complementary sequence of sequence I or a fragment of I in the context of the invention hydridizes under conditions of high stringency defined by a medium containing 50% formamide, 660 mM of sodium chloride, 66 mM of sodium citrate and an incubation for 12 hours at 42° C.

TABLE 1

The B. thuringiensis strain from which the nucleotide sequence I (SEQ ID NO:4) is derived is the strain described in the publication of Lereclus et al. 1988 (FEMS Microbiol. Lett. 49: 417-422).

The replication function, determined by the above sequence, may be modulated by the choice of the promoter. This promoter may be either the promoter present in the 2.6 kb fragment or any promoter capable of functioning in Gram-positive bacteria and preferably is a strong promoter of the veg type (Moran et al., Mol. Gen. Genet. 186: 339-346).

A specific sequence for carrying out the invention, defined by its capacity to hybridize with the complementary sequence of sequence I, is capable of binding to this sequence or a fragment previously mentioned under the conditions of high stringency given above.

In the context of this invention a reverse sequence complementary to a given nucleotide sequence is said to be complementary to this nucleotide sequence. The term “reverse” takes into account the restoration of the 5′—3′ orientation of the nucleic acid which is also complementary to the given base sequence by the nature of the nucleotides it contains.

A sequence called “DNA sequence of interest” is a sequence capable of having economic value or an interest in the context of research, where it is desired to clone or even to express it in a cell host which may be its natural host or even a different strain possessing an interest on account of its properties.

As an sample, among the DNA sequences of interest, mention will be made of the DNA sequence coding for the delta-endotoxins of B. thuringiensis which are responsive for the production of crystals having a toxic activity towards insect larvae. In this connection, the DNA sequences called CryI, CryII, CryIII or CryIV described in the publication by Höfte and Whiteley (1989 Microbiol. Rev. 53: 242-255) or any other Cry gene coding for a delta-endotoxin exhibiting an insecticidal activity are designated more particularly.

Other DNA sequences of interest are sequences which may be produced in Gram-positive bacteria on an industrial scale, for example, by fermentation or other procedures. As examples enzymes such as proteases, lipases and amylases, and protein hormones may be mentioned.

Other sequences of interest are constituted by heterologous sequences with respect to the cell host. For example, mention may be made of sequences coding for bacterial antigens which can be used as immunogens, for viral antigens, for example the HBs antigen or even for parasitic antigens such as those of P. falciparum.

According to a useful embodiment of the invention, the previously defined recombinant vector contains:

either a fragment II included in nucleotide sequence I and characterized in that it is defined by the BalI-AflII sites (nucleotides 1 to 1016) or (SEQ ID NO:5) the BalI-Scal sites (nucleotides 1 to 1076) (SEQ ID NO:6), is about 1 kb long in B. thuringiensis and is capable of ensuring the autonomous replication of the recombinant vector formed,

or a sequence hybridizing with fragment II under conditions of high stringency and,

at least one DNA sequence of interest inserted in phase with the above fragment.

The presence of this fragment designated by II (SEQ ID NO:5 or 6) ensures the autonomous replication of the recombinant vector formed and does so in Gram-positive bacteria whose host proteins are used for this replication.

According to another embodiment of the invention, the recombinant vector contains in phase with a functional promoter in the Gram-positive bacteria,

a DNA fragment (also designated by the term replicon) included in the preceding sequence 1 (SEQ ID NO:4) and in the preceding sequence II (SEQ ID NO:5 or 6), and corresponding to the nucleotide sequence III (SEQ ID NO:7) defined by SpeI-AflII sites comprising the nucleotides 312 to 1016 and a length of about 705 bp in B. thuringiensis or a fragment hybridizing with the sequence complementary to sequence III under conditions of high stringency, or also a modified sequence III, provided that this fragment allows the vector formed to replicate in a Gram-positive bacterium when it is placed under the control of a promoter and,

at least one DNA sequence of interest inserted in phase with the replicon.

In order to be functional as regards the replication of the vector, the nucleotide sequence III (SEQ ID NO:7) must be placed under the control ot a promoter oriented in the same sense as sequence III (SEQ ID NO:7).

The sequences I, II and III (SEQ ID NO:4-7) contain a nucleic acid fragment of about 70 nucleotides, including a symmetric sequence (SEQ ID NO:8) , the centre of symmetry of which is located at nucleotide 390. This sequence included between nucleotides 355 and 424 is imperfectly symmetrical and itself comprises a symmetrical sequence (SEQ ID NO:9) included between nucleotides 395 and 421 whose centre of symmetry is located at position 408.

The efficiency of replication of the recombinant vector according to the invention may be ensured by the use of a promoter in phase with sequence III (SEQ ID NO:7), making possible the autonomous replication of this vector and corresponding to or included in the nucleotide sequence IV (SEQ ID NO:10) defined by the BalI-NdeI sites, comprising the nucleotides 1 to 146 in B. thuringiensis or a promoter constituted by a sequence hybridizing under conditions of high stringency with the sequence complementary to sequence IV, or also a modified sequence IV, provided that it defines a functional promoter under the above conditions, when it is in phase with the replicon.

Another recombinant vector according to the invention is characterized in that it contains, in addition to the sequence III (SEQ ID NO:7) or its derivatives as previously defined:

either a sequence containing elements necessary for the autonomous replication of the recombinant vector formed in a Gram-positive bacterium and elements contributing to the segregational stability of the vector, this sequence corresponding to or being included in the nucleotide sequence V (SEQ ID NO:11 or 12) defined by the BalI-SspI or BalI-SpeI sites comprising the nucleotides 1 to 304 and 1 to 314, respectively, of B. thuringiensis,

or a sequence hybridizing with the sequence complementary to sequence V under highly stringent conditions,

or a sequence modified with respect to sequence V, provided that it conserves the functional properties of autonomous replication and stability of sequence V within the vector.

The invention also relates to a recombinant vector corresponding to one of the definitions described above, characterized in that it contains in addition, a DNA fragment which ensures the stable maintenance of the recombinant vector in a Gram-positive bacterium, this fragment corresponding to

either the nucleotide sequence VI (SEQ ID NO:13) defined by the HaeIII-HpaI sites comprising a length of about 1234 bp between nucleotides 1408 to 2642 of B. thuringiensis, or to any part of sequence VI which contributes to the stable maintenance of the vector in a bacterium, in particular a fragment comprising the HaeIII-AccI sequence at sequence VI of about 351 bp,

or to a DNA fragment modified with respect to the above fragments, provided that it conserves the capacity of sequence VI to confer stability on the vector formed,

or to a fragment hybridizing with the sequence complementary to the above fragments.

The maintenance of the recombinant vector in a Gram-positive bacterium may be important depending on the uses for which this vector is designed.

For example, if Gram-positive bacteria with a vector of the invention comprising a sequence which it is desired to clone or express at a high level are transformed, it is important that the vector be stable. The desired stability may be a structural stability or a segregational stability, this latter being conferred or at least augmented by the presence of sequence VI or a fragment of this sequence under the conditions defined above.

Various vectors can be used to carry out the invention. Recourse will advantageously be had to a vector of the plasmid type and in particular to a vector implicating plasmid elements such as pUC18 or pUC19, in addition to the elements described above.

A recombinant vector according to the invention may additionally contain a specific selection system making it possible to select the Gram-positive bacteria containing the recombinant vector after transformation.

Such a system may be constituted by a gene coding for an enzyme necessary for the metabolism of the transformed bacterium. In this connection, it may be genes responsible for the synthesis of metabolites such as tryptophan, uracil or thymine, or genes responsible for the use of sugars.

The selection system may also be constituted by a gene permitting a coloured selection of the recombinant clones, such as the lacZ or XylE genes or by a gene for resistance to a given antibiotic, for example a gene for resistance to erythromycin or ampicillin.

This last type of selection system is preferably selected when the transformants (bacteria transformed by the vector of the invention) are not intended for dispersal in the environment.

A preferred recombinant vector in the context of the invention is the plasmid pHT315 deposited on Jun. 7, 1991 with the CNCM (Collection Nationale de Cultures de Microorganismes in Paris, France) under number I-1111.

This plasmid which when it is integrated in a bacterium of the B. thuringiensis or B. subtilis type may produce a about 15 copies may also be used as starting plasmid and be modified for example by the incorporation of genes of interest which were discussed above.

Another useful vector in the context of the invention is the plasmid pHT3120 containing the BalI-AflII DNA sequence of about 1000 bp or the BalI-ScaI sequence of about 1076 bp of B. thuringiensis, recombined with the HaeIII-HpaI DNA sequence of about 1234 bp of B. thuringiensis.

In a preferred embodiment of the invention the recombinant plasmid comprises at least two DNA sequences of interest, each one being under the control of a cloning promoter and optionally an expression promoter, functional in Gram-positive bacteria.

The use of nucleotide sequences which have been described in the foregoing pages to clone and optionally express DNA sequences of interest requires that these nucleotide sequences are in the cis position with respect to the DNA sequences of interest.

The invention also refers to the different nucleotide sequences which have been described above under the references I, II, III, IV, V and VI (SEQ ID NO:4-7 and 10-12) and which are defined in the following terms:

a nucleotide sequence I (SEQ ID NO:4) of B. thuringiensis of about 2.6 kb included between the BalI-HpaI sites of the sequence below or,

any fragment included in this sequence provided that it allows the replication of the recombinant vector when it is under the control of a functional promoter in Gram-positive bacteria or,

any sequence hybridizing with the sequence complementary to the above sequence or fragment under highly stringent conditions;

a DNA fragment included in sequence I and characterized in that it is a fragment defined by the BalI-AflII or BalI-ScaI sites (SEQ ID NO:5 or 6) of about 1016 bp (1,016 kb) of B. thuringiensis. capable of ensuring the autonomnous replication of the recombinant vector formed, or any sequence hybridizing with the above fragment under conditions at high stringency;

a DNA fragment or replicon included in sequence I and characterized in that it corresponds to or in that it is included in nucleotide sequence III (SEQ ID NO:7) defined by SpeI-AflII sites comprising the nucleotides 312 to 1016 in Bacillus thuringiensis, or a fragment hybridizing with the sequence complementary to sequence III or even a modified sequence III, provided that this fragment allows the replication of a recombinant vector in which it is integrated in a Gram-positive bacterium when it is in phase with a promoter,

a promoter characterized in that it corresponds to or in that it comprises nucleotide sequence IV (SEQ ID NO:10) defined by the BalI-NdeI sites comprising the nucleotides 1 to 146 in B. thuringiensis, or corresponding to a sequence hybridizing with the sequence complementary to sequence IV or even of a modified sequence IV, provided that the promoter formed conserves its capacity to allow the autonomous replication of a recombinant vector when it is in phase with the replicon;

a nucleotide sequence included in sequence I (SEQ ID NO:4) and itself comprising a promoter containing elements allowing the replication of a recombinant vector containing it in a Gram-positive bacterium and elements contributing to conferring on this vector its segregational stability, characterized in that it corresponds to or in that it is included in sequence V (SEQ ID NO:11 or 12) defined by the BalI-SspI or BalI-SpeI sites comprising the nucleotides 1 to 304 and 1 to 314 in B. thuringiensis, or a sequence which hybridizes under conditions of high stringency with the sequence complementary to sequence V, or even a modified sequence V, provided that it conserves the functional properties of autonomous replication and stability of sequence III;

a DNA fragment capable of conferring on a recombinant vector its capacity to persist in a stable manner in a Gram-positive bacterium or to increase the stability of this vector when it is introduced in a Gram-positive bacterium, characterized in that it corresponds to nucleotide sequence VI (SEQ ID NO:13) defined by the HaeIII-HpaI sites comprising a length of about 1234 bp between the nucleotides 1408 to 2642 in B. thuringiensis or comprising the HaeIII-AccI sequence of sequence VI at abut 351 bp or a fragment modified with respect to the above fragments, provided that it conserves the properties of sequence VI involving the stability of a vector containing it in a Gram-positive bacterium, or even a fragment hybridizing with the sequence complementary to the above fragments.

The invention also relates to a Gram-positive bacterium, characterized in that it is transformed by a recombinant vector complying with the descriptions given in the preceding pages.

These transformed bacteria may be bacteria such as Bacillus thuringiensis or Bacillus subtilis, modified to clone an additional number of copies of DNA sequences coding for example for crystal proteins or delta-endotoxins.

Other bacilli which can be transformed are, for example, B. cereus, B. sphaericus or B. megaterium.

The agents of the invention are thus suited for the construction of recombinant Gram-positive bacteria appropriate for cloning, and optionally for expressing a DNA of interest. Bacteria thus obtained may have uses in industry for producing large quantities of DNA or proteins, for example, in procedures involving fermentation steps to which bacteria such as B. thuringiensis lend themselves, or for the production of compositions for medical use.

The invention relates, in particular, to any recombinant bacterium capable of expressing bacterial antigens or immunogens, viral antigens such as the surface antigen of the hepatitis B virus (HBs), HIV antigens or immunogens, parasitic antigens such as those of P. falciparum.

The object of the invention is also a larvicidal composition active against insect larvae, characterized in that it contains as active ingredient bacteria transformed according to the previously described method in which the sequence of interest is a crystal gene coding for a delta-endotoxin active against the lepidoptera, coleoptera or diptera, in particular the cryI, cryII gene, the cryIII gene or the cryIV gene.

Generally, the recombinant vectors according to the invention can be used for the production of toxins,, in particular polypeptides toxic towards insect larvae and in particular, towards the lepidoptera, coleoptera or diptera, this production of toxins being carried out through the intermediary of microorganisms of the Gram-positive bacteria type.

The strains thus transformed constitute biopesticides Another use of the vectors and nucleotide sequences according to the invention is the cloning of selected DNA sequences. These cloned sequences may then be used in specific cell hosts to construct recombinant strains, for example recombinant E. coli strains.

The procedures for cell transformations, whether bacteria or other types of cells, with the recombinant vector according to the invention are the procedures usually used and such as described in the examples.

It will thus be possible to have recourse to a procedure such as electroporation described by Leredus et al. (1989 FEMS Microbiol. Lett. 60: 211-218).

Other characteristics and advantages of the invention will become apparent in the examples and in the Figures which follow.

DETAILED DESCRIPTION OF THE DRAWINGS

FIG. 1: (1A and 1B): Nucleotide sequence (SEQ ID NO:1) of the BalI restriction fragment of pHT1030 and deduced amino acid sequences of ORF1 (FIGS. 1A and 1B) (SEQ ID NO:3) and ORF2 (FIG. 1A).

The inverted repeat sequences capable of forming a stem and loop structure are underlined by arrows, The −35 and −10 regions of the putative promoter, found in the spaA locus are underlined. The ribasomal binding site and the potential start codon for the translation of spbB are shown in bold characters. The asterisks indicate the stop codon for translation.

FIG. 2: Construction of deletion derivatives of pHT1030 and analysis of their replication and stability in the Bacilli.

The replication origin probe vector pHT181 described in the text is shown. In the upper part of the Figure. The restriction sites used to done the 1.2 kb DNA fragment carrying the Em^(r) gene in pUC18 are in parentheses. The location and orientation of the erythromycin (Em^(r) and beta-lactamase (Ap^(r)) genes are shown by arrows.

The different restriction fragments of pHT1030 cloned into the cloning sites of pHT181 to give the plasmids pHT3103 to pHT3130 are shown under the map of pHT181. These plasmids are constructed by elution of the appropriate restriction fragment from agarose gels and cloning in pHT181 cut by the appropriate enzymes. The recombinant plasmids carry the following restriction fragments: pHT3130, the entire 29 kb BalI fragment of pHT1030, pHT3130 HpaII, the BalI fragment in which the HpaII site is removed (see text); pHT3120, the 1.1 kb BalI-ScaI fragment and the 1.5 kb HaeIII-BalI fragment cloned contiguously; pHT3115, the 2.7 kb NdeI-BalI fragment; pHT3114, the 2.3 kb HaeII fragment; pHT3113a and b, the 1.2 kb SspI fragment; pHT3112a and b, the 2.6 kb SpeI-BalI fragment; pHT3112a and b, the 2.2 kb HindIII-BalI fragment; pHT3110, the 1.1 kb AccI-BalI fragment; pHT3109, the 2.6 kb BalI-HapII fragment; pHT3108, the 2.1 kb BalI-HapII fragment; pHT3107, the 1.7 kb BalI-XhoII fragment; pHT3106, the 1.4 kb BalI-HaeIII fragment; pHT3105a and b, the 1.1 kb BalI-ScaI fragment; pHT3104a and b, the 1 kb BalI-AflII fragment and pHT3103, the 0.7 kb BalI-HindIII fragment. All the constructions have been checked by restriction mapping of the recombinant plasmids. The location and orientation of the ORF1 (SEQ ID NO:1) and ORF2 are shown by a compartment and an arrow, as shown by the nucleotide sequence shown in FIG. 1. The convergent arrows symbolize the groups of inverted repeat sequences p and the arrow indicate the position and the orientation of the lacZ promoter of pUC18.

Construction of the plasmid pHT3120

The plasmid pHT3130 (FIG. 2) is digested, on the one hand, with the enzymes KpnI and ScaI and, on the other, with the enzymes HaeIII and BamHI. The 1.1 kb KpnI-ScaI restriction fragment (containing the BalI-ScaI segment of the replication region) and the 1.5 kb HaeIII-BamHI restriction fragment (containing the HaeIII-BalI segment of the stability region) are obtained and purified separately on agarose gel. The two restriction fragments are ligated together in the presence of the vector pHT181 digested by the enzymes KpnI and BamHI and in the presence of DNA ligase.

The ligation mixture is used to transform the E. coli strain TG1 and the recombinant clones are selected an LB medium containing ampicillin (100 μg/ml) and X-gal. Among the transformants, a white Ap^(r) colony was isolated and the analysis of its plasmid DNA indicates that the clone carries a plasmid with the expected restriction map. This plasmid called pHT3120 does not contain the 0.3 kb ScaI-HaeIII fragment of pHT3130.

The replication of each of the deletion derivatives of pHT1030 was tested by transformation of B. subtilis and B. thuringiensis+ indicates transformant clones resistant to erythromycin were obtained; − indicates that Em^(r) transformants were not obtained. The segregational stability of each of the recombinant plasmids was tested in B. subtilis (B.s) and B. thuringiensis (B.t) in an LB medium as described in Experimental Procedures. The percentages of clones which were Em^(r) after about 25 generations (in the case of B. subtilis) and 40 generations (in the case of B. thuringiensis) without selection pressure have been indicated. NT: not tested.

FIG. 3: Analysis of the production of single-stranded DNA in cells containing deletion derivatives of pHT1030

Cell lysates of B. subtilis containing pHV33 (lanes A and A′), pHT3130 (lanes B and B″) or pHT3104a (lanes C and C′) and of B. thuringiensis containing pHT3130 (lanes D and D) or pHT3104a (lanes E and E′) were separated by agarose gel electrophoresis.

Gel 1 was transferred to a nitrocellulose filter after denaturation and gel 2 without denaturation. The filters were then hybridized with pUC18 labelled with ³²P which contains DNA sequences also present in all of the plasmids analysed. The Figure shows the autoradiographs obtained after exposure. ss, sc, oc and hmw indicate the single-stranded, superhelical, open circle (or dimeric) forms and high molecular weight of the pHV33 DNA, respectively.

FIG. 4: Expression of the spbB gene in an in vitro E. coli transcription-translation system.

The autoradiography of the labelled polypeptides labelled with [³⁵S]-methionine, separated on a 12.5% acrylamide gel produced by: lane 1, pHT181; lane 2, pHT3109; lane 3, pHT3114; lane 4, a 464 bp BstUI fragment isolated from pHT3130 and containing the spbB gene; lane 5, the 462 bp BstUI fragment isolated from pHT3130ΔHpaII and containing an interrupted spbB gene. Erm, Bla and SpbB indicate the gene products of erm, bla and spbB, respectively. The size of the molecular weight markers of the peptides is indicated (kDa).

FIG. 5: Segregation stability of the deletion derivatives of pHT1030 during vegetative growth.

Exponentially growing cells of B. subtilis (table A) and B. thuringiensis (table B) carrying various plasmids were evaluated with respect to their segregational stability in a nonselective BHI medium as described in Experimental Procedures. No significant differences were observed in the growth levels between cells harboring the various plasmids. The symbol for each plasmid is indicated in Table 3.

FIG. 6: Segregation stability of the deletion derivatives of pHT1030 during sporulation.

The stability of the plasmid was evaluated in speculating B. subtilis (table A) and B. thuringiensis (table B) cells carrying various plasmids in a non-selective HCT or SP medium as described in Experimental Procedures. The symbol used for each plasmid is indicated in FIG. 5.

FIG. 7: Construction of the pBC16 variants carrying regions of the spbB locus.

The physical map of the recombinant plasmid pHT1618 is shown in the upper part of the Figure. The replication regions of pBC16 and pUC18 are labelled ori.Bc and ori.Ec, respectively. The positions and orientations of the genes conferring resistance to tetracycline (Tet¹) and ampicillin (Ap¹) are shown by arrows. The restriction sites used for the cloning of pBC16 1 (29kb EcoRI segment whose ends have been filled by the Klenow fragment of the DNA polymerase 1) in pUC18 are in parentheses.

The physical and genetic organization of the BalI DNA fragment is shown in conformity with the results described in the text. spbA and spbB show the positions of the loci. ori.Bt represents the minimal replicon of pHT1030. The other symbols are as described in the legend to FIG. 2.

The full lines represent the segments of the BalI fragment cloned into the cloning sites of pHT1618 to give the plasmids pHT1609 to pHT611. The DNA segments were purified separately on agarose gel and cloned in pHT1618 cut by appropriate enzymes. pHT1611 bears the 2.2 kb HindIII—HindIII fragment isolated from pHTM3130 and corresponding to the 2.2 kb HindIII-BalI fragment of pHT1030 (the second HindIII is derived from the pHT3130 polylinker). pHT1611ΔHpaII bears the 2.2 kb HindIII—HindIII fragment isolated from pHTM3130 HpaII. pHT1610 bears the 1.1 kb AccI-BalI fragment and pHT1609 bears the 1.6 kb ScaI-HpaI fragment of pHT1030. The constructions were checked by restriction mapping of the recombinant plasmids. p and the arrow indicate the position and the orientation of the lacZ promoter of pUC18.

FIG. 8: Stability of the pBC16 variants bearing the spbB regions.

Exponentially growing cells a B. subtilis harboring various plasmids were evaluated with respect to segregational stability in a non-selective BHI medium as described in Experimental Procedures. The symbol of each plasmid is indicated in the Figure.

FIG. 9: Elimination of the HindIII site of pHT1035 and selection of variants with a high copy number.

The HindIII site of pHT1035 was removed as shown in the first part of the Figure. In vitro mutagenesis of pHT1035ΔHindIII was carried out by treatment with hydroxylamine as described previously (Humphreys et al., 1976 Mol. Gen. Genet. 145: 101-108). 20 ug of the treated DNA were used to transform the E. coli strain JM83. Approximately ten thousands Cm-resistant clones (5 μg/ml) were collected and the plasmid DNA was extracted. Subsequently, competent B. subtilis cells were transformed by about 10 μg of plasmid DNA and spread on LB gelose containing 25 μg of Cm per ml. From about one hundred Cm^(r) clones obtained, fourteen were tested for their plasmid content. Agarose gel electrophoresis of the DNA preparations indicated that nine of them harbored plasmids with a number of copies higher than the parent plasmid pHT1035 HindIII. Two clones harboring plasmids with high and intermediate numbers of copies were selected. The arrows above “cat” and “ori.Ec” indicate the direction of transcription of the cat gene and the direction of replication of pBR322, respectively. The double arrow above “ori1030” indicates that the orientation of replication of pHT1030 is not known. The unique restriction sites of the plasmids are shown in bold characters.

FIG. 10: Construction of the shuttle vectors pHT304, pHT315 and pHT370.

The 2.6 kb HpaI-BalI DNA fragment carrying the replication and stability regions of pHT1030 was isolated and purified separately from pHT1035 HindIII, pHT1035-15 HindIII and pHT1035-70 HindIII. A 1.2 kb KpnI-BamHI carrying the constitutive erm gene derived from Tn1545 (Trieu-Cuot et al., 1990 Nucleic Acids Res, 18: 3660) was isolated in the form of a Asp718-BamHI and the ends were made blunt with PolIk. Each HpaI-BalI fragment was cloned at the SspI site of pUC19 with the fragment containing the erm gene by triple ligation. The three ligation mixtures were used separately to transform the E. coli strain JM83, and the recombinant clones were selected on LB gelose plates containing Ap (100 ug/ml) and Er (150 ug/ml). The shuttle vectors pHT304, pHT315 and pHT370 in which the different DNA fragments are cloned at the same place in the sane orientation were selected by restriction mapping. The sites destroyed at the blunt junctions are shown in parentheses. The arrows above “Er^(R)” and “Ap^(R)” and before “lacZpo” indicate the direction of transcription of the erm, bla and lacZ genes, respectively. The number of copies of the plasmid in B. thuringiensis is indicated for each vector. The other symbols are as described in the legend to FIG. 9.

FIG. 11: Analysis of the proteins of the B. thuringiensis transformants expressing the cryIIIA gene.

Spore-crystal preparations were obtained and analysed by SDS-PAGE and stained with Coomassie Blue as was described previously (Lerecus et al., 1989a FEMS Microbiol. Lett. 60: 211-218). An aliquot sample (20 μl) was loaded into each well. Lanes 1, 2, 3, 4: kurstaki HD1 CryB strain containing pHT315; pHT304 cryIIIA; pHT315 cryIIIA and pHT370 cryIIIA, respectively. Lane 5: molecular weight markers. The arrows indicate the crystal components of 73 and 67 kDa

EXAMPLES 1st Example ANALYSIS OF THE NUCLEOTIDE SEQUENCE OF THE REPLICON pHT1030

The 2.9 kb BalI DNA fragment containing the replication region of pHT1030 (Leredus et al., 1988 FEMS Microbiol. Lett. 49: 417-422) was inserted in both orientations at the SmaI site of the pUC18 vector and different DNA fragments were subcloned into the phages M13mp18 and M13mp19 for sequencing. Overlapping deletions were also obtained from the entire BalI fragment cloned in M13mp19 using the procedure of Dale et al.(1985, Plasmid 13: 31-40). The synthesis of specific oligonucleotide primers, deduced from the results of preliminary sequencing has made it possible to obtain more information concerning the sequences starting from suitable recombinant phages used as matrices. The complete nucleotide sequence (FIG. 1) (SEQ ID NO:1) of the 2872 bp BalI fragment was determined on both DNA strands. The total dA+dT content of the DNA fragment of 63% is very similar to that of the B. thuringiensis chromosome: 63.6% (Kaneko et al., 1978 Microbiol. Immunol. 22: 639-641).

The sequence comprises two major complementary inverted repeat sequences which were able to form potentially stable hairpin loop RNA structures. The largest of the two regions comprises 70 nucleotides with a centre of symmetry situated at nucleotide 390. The free energy of interaction calculated according to Tinoco et al. (1973, Nature (London) New Biol. 246: 40-41) is −156.5 kJ/mole. The two symmetric sequences are repeated imperfectly and the mapping of the DNA region in FIG. 1A between the positions 392 and 425 itself contains a pair of inverted repeat sequences having a calculated free energy of interaction of −66.1 kJ/mole. The second major group of complementary sequences is situated between the positions 1572 and 1598. Eleven nucleotides are repeated perfectly and can form a hairpin loop structure with a calculated free energy of interaction of −95.4 kJ/mole.

The nucleotide sequence shown in FIG. 1A (SEQ ID NO:1) was examined in both directions for the regions coding for a potential protein. The latter were defined on the basis of dimensions (>70 codons) and suitable translation initiation signals (McLaughlin et al., 1981 J. Biol. Chem 256: 11283-11291). Only two supposed open reading frames (ORF open reading frames) were found, they code in opposite directions (FIG. 1). The presumed start codons of ORF1 (UUG) and ORF2 (AUG) are preceded by appropriate ribosomal binding sites corresponding to the 3′—OH of the 16S r RNA of B. subtilis (McLaughlin et al., 1981). The free energies of interaction, deduced according to Tinaco et al.(1973) are −57.5 kJ/mole (ORF1) and −51 kJ/mole (ORF2). ORF1 codes for 134 amino acids starting at position 2193 and terminating at position 1792 (SEQ ID NO:3). The calculated molecular mass of the supposed ORF1 product is 15524. ORF2 codes for a polypeptide (SEQ ID NO:2) starting at position 2521, interrupted at position 2872 by cloning of the BalI DNA fragment.

Comparison of the deduced ORF1 and ORF2 sequences with the sequences (SEQ ID NO:3 and 2) of proteins available in the Gene Libraries/EMBL and NBRF, and specifically those encoded in plasmids, did not reveal any significant homology.

Potential promoters for ORF1 and ORF2 have been identified by comparison of the regions upstream from ORF1 and ORF2 with known consensus regions of B. subtilis promoters (Moran, 1986 Regulation a Procaryatic Development. American Society for Microbiology, Washington D.C., 167-184) (FIG. 1). The region of symmetry situated between positions 1572 and 1598 may correspond to a transcription terminator for ORF1. When it is read on the same strand as ORF1, the potential hairpin loop RNA structure is followed by a segment of 6 U residues interrupted by two A residues. This structure is reminiscent of a rho-independent terminator.

DETERMINATION OF THE MINIMAL REPLICATION REGION OF pHT1030.

To test the replication activity of DNA fragments derived from the BalI fragment of pHT1030, the replication origin probe vector pHT181 was constructed, in which a 1.2 kb DNA fragment carrying a gene conferring resistance to erythromycin on Gram-positive bacteria (Trieu-Cuot et al., 1990 Nucleic Acids Res. 18: 3660) was cloned at the SspI site of pUC18 (FIG. 2). Like pUC18, pHT181 can be used fo cloning experiments in E. coli, given that the Em^(r) gene inserted at the I site interrupts neither the cloning sites of the polylinker nor the beta-lactamase gene. Thus, the entire BalI DNA fragment and several fragments of the latter were cloned in pHT181, and their replication was tested in B. subtilis and B. thuringiensis (FIG. 2). The smallest DNA segment capable of supporting the replication of recombinant plasmids in the Bacilli was a 705 bp SpeI-AflII (nt 312-1016, FIG. 1 (SEQ ID NO:7)). However, the replication capacity of this DNA segment was dependent on its orientation with respect to the lacZ promoter of pUC18. pHT3112a and pHT3113a were capable of transforming Bacilli for resistance to erythromycin, but transformants were not obtained with pHT3112b, pHT3133b, pHT3114 and pHT3115 in which the fragment is in the opposite orientation.

This result suggests that, in the case of pHT3112a and pHT3113a, the lacZ promoter region situated upstream from the cloning sites provides a promoter activity which had been lost in these deletion derivatives. The essential promoter for the autonomous replication of pHT1030 might then be present in the 146 bp BalI-NdeI DNA fragment (nt 1-146), FIG. 1 (SEQ ID NO:10)). Possible −35 (TTGATI) and −10 (TAAAAT) regions are found in this DNA segment at nucleotide positions 75-80 and 98-103, respectively (FIG. 1) (SEQ ID NO:10) . This is in agreement with the fact that the BalI-AflII and BalI-ScaI fragments of 1 kb (SEQ ID NO:5 and 6) provide efficient replication in the Bacilli when they are cloned in one or other orientation in pHT181 to give the plasmids pHT3104a,b and pHT3105a,b (FIG. 2). Thus, the minimal region of pHT1030 conferring autonomous replication is completely included in the 1016 bp BalI-AflII restriction fragment (SEQ ID NO:5) cloned in the plasmids pHT3104a,b (FIG. 2). The two major characteristics of this replication region are the presence at the sequence 70 nucleotides long and symmetrical about a point, and the apparent absence of any protein encoded by a plasmid and required for replication. The longest ORF (95 codons) found in this DNA region does not exhibit an appropriate translation initiation signal.

REPLICATION BEHAVIOUR OF THE DELETION DERIVATIVES OF pHT1030.

The integrity of the replication functions of the minimal replicon cloned in pHTI3104a was verified by comparison at its replication characteristics with those of pHT3130, which is the entire BalI DNA fragment cloned in the replication origin probe vector pHT181 (FIG. 2).

The number of copies of the two plasmids was determined. In both B. subtilis and B. thuringiensis pHT3130 and pHT3104a showed an identical number of copies estimated at 42+/−0.6 covalently closed circular plasmid molecules per chromosome equivalent. It may be concluded that the required functions for the control of the number of copies are all present in the minimal replicon cloned in pHT3104a.

Another approach to test the integrity of the replication functions of pHT3104a consisted in determining its production of single-stranded DNA. Many plasmids derived from Gram-positive bacteria replicate by a mechanism of the “rolling circle” type and the deletion of the negative origin sequence leads to the accumulation of single-stranded plasmid DNA (Gruss and Ehrlich, 1989 Microbiol. Rev. 53: 231-241; Devine et al., 1989). pHT3100 and pHT3104a were tested for the production of single-stranded plasmid DNA by using the procedure described by te Riele et al. (1986a Proc. Natl. Acad. Sci. USA 83: 2541-2545). Total DNA preparations were loaded on to agarose gels, separated and transferred on to nitrocellulose filters with or without prior denaturation with NaOH.

The results of their hybridization with a pUC18 plasmid labelled with ³²P are presented in FIG. 3. pHT3130 and pHT3104a did not produce detectable quantities of single-stranded DNA in either B. subtilis or B. thuringiensis. Furthermore, Gruss and Ehrlich (1988) showed that the insertion of foreign DNA into plasmids of the “rolling circle” type leads to the formation of multimers in tandem of high molecular weight (HMW). By comparison with the hybrid plasmid pHV33 of the “rolling circle” type, significant quantities of HMW were not found with pHT3100 and pHT3104a in B. subtilis (FIG. , lanes B and C) and only low levels when these plasmids were in B. thuringiensis (FIG. 3, lanes D and E). These results strongly suggest that pHT1030 and its deletion derivatives do not replicate by a single-stranded DNA intermediate and show that the replication behaviours of pHT3130 and pHT3104 are not significantly different in B. subtilis and B. thuringiensis. Thus, it may be concluded that the essential replication functions of pHT1030 are conserved in the minimal replicon cloned in pHT3104a.

SEGREGATIONAL STABILITY OF THE DELETION DERIVATIVES OF pHT1030.

To determine the DNA regions necessary for the segregational stability of pHT1030, the maintenance of a selection of the deletion derivatives Rep⁺ of this replicon was characterized in B. subtilis or B. thuringiensis in an LB medium without antibiotic selection (FIG. 2).

The most striking instability results from the deletion of small BalI-SspI or BalI-SpeI DNA fragments (SEQ ID NO:11 or 12). pHT3112a and pHT3113a from which these fragments are missing were rapidly lost in the absence of selection pressure. Consequently, this short DNA fragment, which has been shown above to be linked to the replication function of pHT1030, is also implicated in the stability of the replicon. This region of 300 bp has been designated spbA (stability of the plasmid in the Bacilli).

The other Rep⁺ plasmids were more stable in B. thuringiensis than in B. subtilis. This effect of the host will be discussed hereafter.

Independently of the host bacterium, a partial deletion of ORF2 (pHT3109) and a deletion of the ScaI-HaeIII fragment (pHT3120) gave plasmids as stable as pHT3130. However, the plasmids in which ORF1 is partially or totally deleted (pHT3108 to pHT3104) show a significantly reduced stability. These results suggest that the 1234 bp HaeIII-HpaI DNA fragment containing ORF1 is involved in the maintenance of pHT1030 in the two species of Bacilli. This locus is designated SpbB. To determine whether a potential spbB gene product is responsible or not for the stability of pHT1030, a plasmid bearing an interrupted spbB gene was constructed. The unique HpaII site of the 2.6 kb BalI fragment of pHT1030 was removed by cutting with HpaII and filling of the ends using the Klenow fragment of DNA polymerase I, and the modified BalI fragment was cloned in pHT181 to give the plasmid pHT3130 HpaII. The modification of the restriction site was confirmed by nucleotide sequencing by using a suitable synthetic oligonucleotide primer. Whereas mutagenesis ought to lead to the addition of 2 bp, nucleotide sequencing revealed that, for unknown reasons, 2 bp were lost from pHT3130ΔHpaII (SEQ ID NO:14), (the DNA sequence 5′-TAAATGGGA-3′ has replaced 5′-TAAATCCGGGA-3′ at the nucleotide positions 2070-2080). Nonetheless, this modification causes a shift in the reading frame in the presumed spbB gene (ORF1) moving a nonsense codon 14 codons upstream in the reading frame pHT3130 HPaII had a lower segregational stability than pHT1030 and one similar to that of the deletion derivatives pHT3108 to pHT3104 (FIG. 4).

These experimental data might point to the implication of a polypeptide encoded in spbB in the maintenance of pHT1030 in the Bacilli. The expression of the spbB was tested in an in vitro E. coli. transcription-translation system (FIG. 4). A 564 bp BstUI DNA fragment (located between the nucleotide positions 1692 and 2256 of FIG. 1) containing the supposed spbB gene was purified separately from each of pHT3130 and pHT31304HpaII and was tested in parallel. Only the BstUI DNA fragment from pHT3130 directed the expression of an additional protein of 15 kDa (FIG. 4, lane 4). Furthermore, the in vitro transcription-translation of the entire plasmids pHT3109 and pHT114 led to the appearance of a protein exhibiting the same apparent size. This protein was absent from the assay containing pHT181. The apparent size of the SpbB polypeptide is in agreement with the molecular weight calculated from the nucleotide sequence at ORF1. These results demonstrate that the integrity of this DNA sequence is required for the stability, and probably for the expression, of the encoded protein.

Since the absence of spbB does not affect the apparent replication behaviour of the plasmids, the spbB gene product is only implicated in stability.

Does the locus have an active stabilizing function?

Nordström and Austin (1989, Annu. Rev. Genet. 23: 37-69) defined two classes of stability factors: those which ensure a random distribution of the plasmid during cell division and those which lead to a better than random stability.

In order to determine to which class the spbB locus belongs, it was consequently necessary to establish the frequency of loss of plasmids per generation in the absence and presence of spbB. Comparison of these frequencies with the theoretical frequency based on the number of copies of pHT1030 enabled the role of spbB to be pinpointed.

The stability experiments performed in LB medium have shown the overall maintenance of the plasmids under nonselective conditions (FIG. 2). However, they did not enable the loss frequency of plasmids per generation to be estimated. An overnight culture in an LB medium causes the sporulation at some of the cells. When they were evaluated after about 25 generations, the values obtained for the stability of the plasmids result from a mixed population of vegetative and sporulating cells.

In order to distinguish the stability of the plasmids in the two growth states, the production of cells free from plasmids was followed separately in a rich medium (BHI) in order to prevent the triggering of sporulation and in media specific for sporulation (SP or HCT) in order to determine the frequency of production of a plasmid-free spore.

In BHI medium, the plasmids bearing the spbB locus and the entire replication region (pHT3130, pHT3120 or pHT3109) were maintained in a very stable manner, in view of the fact that more than 95% of the B. subtilis cells harbored these plasmids after 60 generations (FIG. 5A) and 99% of the B. thuringiensis cells after 80 generations (FIG. 5B. The plasmids from which spbB was missing (pHT3104a and pHMT3107) and those in which the spbB gene was ruptured (pHT3108 and pHT3130ΔHpaII) were significantly less stable than the replicons bearing the entire spbB sequence (FIGS. 5A and B).

A second class of plasmids (pHT3112a and pHT3113a) in which the spbA locus is absent appears to be very unstable in both B. subtilis and B. thuringiensis. However, the presence of the DNA region carrying the spbB sequence (pHT3112a) the reduces the instability, as compared with its absence (pHT3113a).

The determination of plasmid stability during sporulation was carried cut by using SP and HCT media in which B. subtilis and B. thuringiensis sporulate synchronously. Just before t₀ of sporulation (about 15 generations after inoculation of the medium without antibiotic), the proportion of Em^(r) cells is unchanged or only slightly reduced (FIGS. 6A and B). This is in marked contrast with the results observed after complete development of the sporulation phase. The cells harboring the plasmids pHT3130ΔHpaII, pHT3108 and pHT3104a give rise to a large promotion of plasmid-free spores, in particular in B. subtilis. The plasmids pHT3130, pHT3120 and pHT3109 are maintained stably during the sporulation process. These results are in agreement with those obtained in vegetative growth and strongly suggest that during sporulation the stability of the plasmids is dependent on the DNA region carrying spbB.

After t₀ of sporulation there is no significant new cell growth. The instability of pHT3130ΔHpaIl, pHT3108 and pHT3104a consequently result from the sporulation stage which may be considered as being a simple cell division. One of the first steps in this differentiation process is the formation of the sporulation septum which divides the cell into two unequal compartments. In both B. subtilis and B. thuringiensis the presporal compartment represents about one sixth of the volume of the parent cell (Ryter, 1965; Ribier and Lecadet, 1973). Thus, it ought to be expected that a random distribution of the plasmids would lead to a high production frequency of plasmid-free spores.

On the basis of the mean of the stability results obtained in the vegetative phase (FIGS. 5A and B) or in the sporulation or phase (FIG. 6A and B), the stability frequencies of the plasmids carrying the spbB locus or lacking this locus were determined and compared with the theoretical frequencies expected with a plasmid having a number of copies at 4.2 per chromosome equivalent, i.e. about 20 copies per cell prior to division (Table 1). Owing to the difficulty of extracting DNA from Bacilli at stage to a sporulation, the plasmid copy number was not measured during this differentiation step and the hypothesis has been put forward that it is identical with that obtained during the vegetative phase.

As shown above, it appears that all of the plasmids are about 4 times less stable in B. subtilis and B. thuringiensis.

Although the calculated number a copies and the apparent behaviour of pHT3104a has ben found to be similar in the two organisms, the stability difference between B. subtilis and B. thuringiensis for this type of plasmid, could result partially from errors in replication control leading to a variation in the number of copies in a population of B. subtilis cells. Nonetheless, other factors relating to the host must probably be considered in order to explain the considerable difference in the stability of the plasmids observed between sporulating cells of B. subtilis and B. thuringiensis (FIG. 6 and Table 1). However, in both B. subtilis and B. thuringiensis the plasmids carrying the spbB region were maintained with higher frequencies than the plasmids not carrying this region (Table 1).

Furthermore, during sporulation, the spbB+ plasmids are maintained with frequencies similar to those deduced from random distribution. These results indicate that in all cases, the presence of spbB diminishes the frequency of loss of the plasmids by a factor of about 20.

Examination of the stability mechanism regulated by spbB

The capacity of spbB to stabilize a heterologous replicon or to function in trans, and its effect on bacterial growth were examined in order to obtain information concerning the mechanism of spbB.

In order to test the capacity of spbB to stabilize a heterologous plasmid the vector pHT1618 was constructed by cloning the replicon pBC16Δ1 (Polak and Novick, 1982) at the SspI site of pUC18 (FIG. 7). pBC16 1 is a derivative at replicon pBC16 of B. cereus which confers resistance to tetracycline on Gram-positive bacteria pBC16 is a plasmid of the “rolling circle” type (Gruss and Ehrlich, 1989 Microbiol. Rev. 53: 231-241).

Different DNA fragments containing the intact or interrupted spbB region were cloned into the cloning sites of pHT1618 (FIG. 7). The stability of these recombinant plasmids was analysed in B. subtilis during vegetative growth without antibiotic (FIG. 8). pHT1610 and pHT1611ΔHpaII were less stable than pHT1618. This reduction in stability is in agreement with the preceding data showing that the segregational stability of the plasmid pUB110, which is related to pBC16 (Polak and Novick, 1982), depends on the size and is considerably reduced by DNA insertions (Bron et al., 1988). The instability of pHT1610 clearly indicates that the AccI-BalI fragment containing the spbB gene has not conferred a stability function on the replicon.

The addition of DNA segments (ScaI-AccI or HindIII-AccI) situated upstream from the spbB gene to the plasmids completely suppressed the reduction in stability due to the cloning of the spbB gene in pHT1610. In fact, pHT1609 and pHT1611 are at least as stable as pHT1618 and significantly more stable than pHT1610 and pHT1611ΔHpaII which carry DNA insertions of similar dimensions. The determinations of the production frequency of a plasmid-free spore in an SP medium gave similar results.

Consequently, these results show that, in addition to the spbB gene, the ScaI-AccI DNA fragment situated upstream from the gene is necessary to confer stability on recombinant plasmids derived from pBC16. The deletion of the ScaI-HaeIII fragment does not diminish the stability (pHT3120) and, consequently, the essential function for stability resides in the short HaeIII-AccI fragment. This DNA segment contains the region of symmetry, a potential terminator, which may be required for the functional expression of the spbB gene product.

In order to determine whether the spbB proton is transacting or not, B. subtilis Rec⁻ strains harboring pHT1618 or pHT1609 were transformed by the unstable plasmids pHT3104a or pHT3130 HpaII. pHT1609 had no detectable effect on the stability of these two plasmids indicating that the stabilization requires that the replicon and the spbB locus are in the same molecule.

Hence spbB would appear not to be a true partition system in which the proteins function in trans in order to ensure the distribution of the plasmid to the daughter cells (Austin and Nordström, 1990 Cell 60: 351-354). This characteristic and the capacity to stabilize a heterologous replicon are analogous to those of the “killer” systems ccd and hok/sck (Jaffé et al., 1985 J. Bacteriol. 163: 841-849; Gerdes et al., 1986 Proc. Natl. Acad. Sci. USA 83: 3116-3120). Interestingly, the B. subtilis cells which harbor spbB⁺ plasmids produce only about a third of the number of viable spores compared with those harbouring spbB⁻ plasmids (Table 2). This is also in agreement with a model of the action of the “killer” type.

If it is supposed that, during sporulation the B. subtilis cells, the high production frequency of a plasmid-free spore is equivalent with spbB⁻ and spbB⁺ plasmids, the apparent stability of the spbB⁺ plasmids might consequently result from a post-segregational activity of the SpbB protein. When the spbB⁺ plasmid is lost, the SpbB protein may become functional and its physiological effect might be to prevent or delay cellular development and the formation of viable spores.

DISCUSSION

The replication and stability functions of the Gram-positive plasmid pHT1030 were first localized on the map at a 2.9 kb BalI restriction fragment (SEQ ID NO:1) (Lereclus et al., 1988 FEMS Microbiol. Lett. 49: 417-422).

The construction of the deletion derivatives of pHT1030 reveals that the minimal replicon conferring autonomous replication is included in a 1 kb DNA fragment. The plasmids carrying this DNA region show a replication behaviour similar to that of the plasmids carrying the entire BalI restriction fragment. These are plasmids with a low copy number (42 copies per chromosome equivalent) and they do not accumulate single-stranded DNA molecules during replication. This latter characteristic excludes a “rolling circle” mode of replicating which is found most commonly in Gram-positive replicons (Gruss and Ehrlich, 1989 Microbiol. Rev. 5: 231-241).

The principal characteristic of this 1 kb DNA fragment is the absence of a sequence coding for a potential protein. Consequently, it resembles plasmids of the ColE1 type which only require host proteins for their own replication. Nonetheless, unlike ColE1, the plasmids derived from pHT1030 are not amplified after addition of chloramphenicol to the culture medium. These characteristics indicate that pHT1030 is located in a class of replicons which has not previously been found in the Gram-positive bacteria.

Another special characteristic of the minimal replicon of pHT1030 is a sequence (SEQ ID NO:8) of 70 nucleotides forming potentially a hairpin loop RNA structure in which one of the two complementary regions itself contains an inverted repeat sequence (mapping between the nucleotide positions 392 and 425 in FIG. 1).

The deletion of a 300 bp DNA region containing a potential promoter (which might be essential for the synthesis of the initiator RNA molecule) makes the pHT1030 derivatives incapable of replicating. This defect is suppressed by the addition of the lacZ promoter region of pUC18, but the segregational stability of the resulting plasmids (pHT3112a and pHT3113a) is seriously diminished in B. subtilis and B. thuringiensis. Consequently, this 300 bp segment defines a stability locus (spbA) probably linked to the replication function of pHT1030.

The segregational stability of the various deletion derivatives of pHT1030 was examined separately during vegetative growth and the sporulation phase. The experiments indicate that the plasmids carrying the minimal replicon of pHT1030 or the plasmids deficient in the DNA region designated spbB are not maintained in a stable manner in the Bacilli, in particular in B. thuringiensis. For unknown reasons, the stability of these plasmids is worse than random in B. subtilis. Interestingly, it has been shown that the high frequency of production of a plasmid-free spore could be correlated with a random distribution of the plasmids on the basis of unequal division of the cell by the sporulation septum However, in both the vegetative phase and sporulation the plasmids carrying the spbB locus are maintained stably in the two species of Bacilli.

spbB codes for a polypeptide of 15 kDA which might be implicated in the stability of pHT1030. Once cloned in a heterologous replicon (derived from pBC16), the spbB locus confers a low but significant segregational stability, whereas an spbB⁺ plasmid does not stabilize in trans plasmids from which spbB has been deleted or which carry an interrupted spbB gene. This indicates that the spbB locus must be linked to the replicon in order to exert its stability function.

spbB is thus actively implicated in the segregational stability of pHT1030, independently of the replication function. The mechanism by which it functions exhibits characteristics resembling those of the “killer” systems ccd and hok/sok (Jaffé et al., 1985 J. Bacteriol 163: 841-849; Gerdes et al., 1986 Proc. Natl. Acad.Sci. USA 83: 3116-3120). The plasmids carrying such loci produce a killer protein and an antagonistic agent which is a protein in the ccd system (Ogura and Hiraga, 1983 Proc. Natl. Acad. Sci USA 80: 4784-4788; Miki et al., 1984 J. Mol. Biol. 174: 605-625), and an anti-sense RNA in the hok/sok system (Gerdes et al., 1990 Mol. Microbiol. 4: 1807-1818). When the plasmids are lost the blocking agent disappears more rapidly than the more stable killer determinant, permitting the expression of the killer activity which causes cell death.

The analogy between spbB and the killer mechanism is reinforced by the results obtained under conditions (sporulation in B. subtilis) leading to a high production frequency of spores free from plasmids. The production of viable spores is strongly reduced when the cells harbor an spbB⁺ plasmid. This would be expected if the SpbB protein had a killer-type effect. However, no homology has been found between SpbB and the killer proteins CcdB and Hok, and the physiological function of SpbB has still to be characterized.

EXPERIMENTAL PROCEDURES

Bacterial strains and growth conditions

The E. coli K-12 strain TG1 [Δ(lac-proAB) supE thi hdsD5 (F traD36 proA⁺ proB⁺ lacI9lacZΔM15)] was used for the cloning and sequencing experiments. The B. subtilis strain 168 (trpC2) (Anagnostopoulos and Spizizen, 1961 J. Bacteriol. 81: 741-746) and the B. thuringiensis strain kurstaki HD1 cryB were used for the replication and stability assays E. coli, B. subtilis and B. thuringiensis were transformed as described by Cohen et al. (1972 Proc. Natl. Acad. Sci. USA 69: 2110-2114), Anagnostopoulos and Spizizen (1961 J. Bacteriol. 81: 741-746) and Lereclus et al. (1989a FEMS Microbiol. Lett 60 211-218).

A Luria broth (LB) was used for the E. coli cultures and preliminary stability assays with B. subtilis and B. thuringiensis. The stability of the plasmid in vegetative growth was determined in a brain-heart infusion (BHI, Difco) in the case of the two Bacilli, and the stability assays during sporulation was carried out in a HCT medium (Lecadet et al., 1980 J. Gen. Microbiol. 121: 203-212) in the case of B. thuringiensis and in an SP medium in the case of B. subtilis. The SP medium containing 8 g of nutrient broth (Difco) per liter, 1 mM MgSO₄, 13 mM KCl and 10 μM MnCl₂ supplemented after sterilization by 1 μM FeSO₄, 1 mM CaCl₂ and 1 g glucose.

The antibiotic concentrations for bacterial selection were the following: ampicillin, 100 μg/ml; erythromycin, 25 μg/ml in the case of the Bacilli and 125 μg/ml in the case of E. coli, and tetracycline, 10 μg/ml.

Plasmids

The plasmid pUC18 in which the 2.9 kb BalI restriction fragment of pHT1030 (SEQ ID NO:1) was inserted at the SmaI site and the plasmid pHT1031 (Lereclus et al., 1988 FEMS Microbiol. Lett. 42: 417-422) were used as DNA source to construct the various deletion derivatives of pHT1030 used in this study. These plasmids are described in FIG. 2 and FIG. 7.

The bifunctional vector pHV33 is composed of pBR322 and pC194 (Primrose and Ehrlich, 1981 Plasmid 6: 193-201). pBC16Δ1 is derived from the plasmid pBC16 of B. cereus (Bernhard et al., 1978 J. Bacteriol. 133: 897-903)

Stability assays

Preliminary stability assays in an LB medium were carried out as previously described (Leredus et al., 1988 FEMS Microbiol. Lett. 492: 417-422).

The bacterial strains containing plasmids to be tested for segregational stability in vegetative growth were inoculated in the selective BHI medium and incubated overnight at 30° C. The cultures were then subsequently diluted 10⁶ fold in a BHI medium without antibiotics and incubated at 37° C. The cultures were diluted (10⁵ to 10⁶ fold) in a fresh non-selective BHI medium every 15 to 20 generations. At regular intervals (about 20 generations) culture samples were spread on nonselective gelose dishes after suitable dilutions. About 100 colonies of each sample were spread with a tooth pick on gelose plates containing the appropriate antibiotic to determine the proportion of bacteria containing plasmids. The segregational stability of the unstable spbA⁻ plasmids (pHT3112a and pHT3113a) was estimated by spreading samples of the recovered cultures at intervals of about 5 generations on both a selective and non-selective gelose medium after suitable dilutions.

For the stability assays during the sporulation phase overnight cultures in the selective BHI medium were diluted 10³ fold in a specific sporulation medium (SP or HCT) containing erythromycin (5 μg/ml) and incubated for 2 to 3 hours at 37° C. The cultures were then diluted 10³ fold in a fresh non-selective HCT or SP medium (zero time) and incubated at appropriate temperatures (30° C. for B. thuringiensis and 37° C. for B. subtilis). After about 15 generations (just before t₀ of sporulation) the samples were used to determine the fraction of cells containing plasmids as described above. After 24 or 36 hours, when most of the spores have been released, the culture samples were heated at 80° C. for 10 minutes to kill the non-sporulating cells. The proportion of spores containing plasmids was then determined as above.

Determination of the plasmid copy number

The plasmid copy number was determined by densitometry of photographic negatives obtained from electrophoretic gels stained with ethidium bromide. The method and the parameters used for the determination of the copy number were as described by Projan et al. (1983 Plasmid 9: 182-190). The size of the B. subtilis and B. thuringiensis chromosomes used to calculate the copy number was 4.2×10³ kb.

Analysis of single-stranded DNA production

Crude plasmid preparations were subjected to electrophoresis on agarose gels and transferred to nitrocellulose filters with or without denaturation (BA85, 0.45 μm, Schleicher and Schuell) as previously described by te Riele et al. (1986a EMBO J. 5: 631-637) for the B. subtilis cells. The filters were hybridized with pUC18 labelled with ³²P.

Materials and DNA sequencing

Restriction enzymes, T4 DNA ligase and the Klenow fragment of DNA polymerase I were supplied by New England Biolabs, Inc. The restriction enzyme Asp178 (used to cut at KpnI sites) and calf intestinal alkaline phosphatase were obtained from Boehringer Mannheim. All of the enzymes were used in accordance with the manufacturers' directions. DNA restriction fragments were purified on agarose gels using a Gene Clean kit (Bio101).

The nucleotide sequencing was carried out by the chain termination method (Sanger et al., 1977 Proc. Natl. Acad. Sci. USA 74: 5463-5467) using the Sequenase sequencing kit purchased from U.S. Biochemical Corp., and [alpha⁻³⁵S]-dATP (110 TBq/mmole) supplied by Amersham Corp. Overlapping deletions were obtained according to the procedure of Dale et al. (1985 Plasmid 11: 31-40) using the Cyclone system as indicated by the manufacturer (International Biotechnologies InC.).

The DNA sequence described here will appear in the EMBL library of nucleotide sequences under the entry number X59245.

In vitro transcription-translation assays were carried out with/³⁵S/-methionine (37 TBq/mmole) from Amersham Corp. with the DNA EXpression System of New England Nuclear, as indicated by the supplier. Radiolabelled proteins were resolved in 12.5% polyacrylamide gels (weight/volume).

Computer analysis

The programs were used on a Data General MV8000 ccmputer. The DNA and amino acid sequences were analysed with the programs used at the Pasteur Institute.

TABLE 1 Plasmid stability in the vegetative and sporulation phases Generation frequency of plasmid-free cells Generation of plasmid-free spores in the vegetative phase(a) in the sporulation phase(b) Theoretical Theoretical probability probability Plasmid B. subtilis B. thuringiensis (½)^(Zn) B. subtilis B. thuringiensis (⅚)^(Zn) pHT3130ΔHpaII 7 × 10⁻³ 2 × 10⁻³ 10⁻⁶ 8 × 10⁻¹ 1.8 × 10⁻¹ 2.2 × 10⁻² pHT3108 pHT3104a pHT3130 4 × 10⁻⁴ 10⁻⁴ 10⁻⁶ 5 × 10⁻² <10⁻² 2.6 × 10⁻² pHT3120 pHT3109 (a)Frequencies determined from FIGS. 5A and 5B. The number of Em^(s) cells at a given time divided by the corresponding number of generations. The results correspond to the mean of the data obtained with the plasmids indicated. (b)Frequencies determined from FIGS. 6A and 6B. The generation frequence of a plasmid-free spore was estimated as the proportion of spores giving rise to Em^(s) colonies. The results correspond to the mean of the data obtained with the plasmids indicated. (c)The theoretical probability depends on the size of the cellular compartment under consideration and the number of copies of the plasmid per cell (2n = 20).

TABLE 2 Effect of spbB on the sporulation of B. subtilis Total number of viable spores Percentage of Plasmid Genotype (per ml)(a) Em^(r) spores(b) pHT3130 spbA⁺spbB⁺   2 × 10⁻⁸ 96% pRT3120 spbA⁺spbB⁺ 2.5 × 10⁻⁸ 95% pHT3109 spbA⁺spbB⁺   3 × 10⁻⁸ 96% pHT3130ΔHpaII spbA⁺spbB⁻   7 × 10⁻⁸ 18% pHT3108 spbA⁺spbB⁻ 6.5 × 10⁻⁸ 30% pHT3104a spbA⁺spbB⁻   8 × 10⁻⁸ 15% (a)The number of viable spores was estimated by spreading dilutions of sporulating cultures on non-selective agar plates, after incubation at 80° C. for 10 minutes. The sporulating cultures were obtained in a selective SP medium. (b)The percentage of Em^(r) spores was estimated by repicking about 100 colonies on agar plates containing erythromycin.

2nd Example CONSTRUCTION OF SHUTTLE VECTORS

Experimental part and discussion

A) Shuttle vectors with different copy numbers

1) Removal of the HindIII site fran pHT1035

pHT1035 is a 6.3 kb plasmid carrying the replication region of plasmid pHT1030 of B. thuringiensis (2.9 kb BalI DNA fragment (SEQ ID NO:1)), a HindIII-BalI DNA fragment carrying the cat gene of pJH101 (Ferrari et al., 1983 J. Bacteriol. 1:1513-1515) and the origin of replication of pBR322 (FIG. 9) (Lereclus et al., 1988 FEMS Microbiol. Lett. 49: 417-422). The unique HindIII site of pHT1035 was removed (FIG. 9) in order to prevent any duplication of the pUC19 restriction sites (Yanisch-Perron et al., 1985 Gene 33: 103-119) used for the construction of the shuttle vectors. The modification at the HindIII site does not disturb the replication and stability functions of the plasmid, since pHT1035ΔHindIII was capable of transforming B. subtilis strain 168 (Anagnostopoulos and Spizizen, 1961 J. Bacteriol. 81: 741-746) in Cm^(R) (10 μg/ml) and was maintained stably without selection pressure (90% of the cells contained the plasmid after about 25 generations in a non-selective LB medium).

2) Selection of the high copy number derivative of pH1035 HindIII

The DNA of plasmid pHT1035 HindIII was treated with hydroxylamine (FIG. 9) and was then used to transform E. coli cells in order to recover plasmid DNA molecules (multimer forms) capable of transforming B. subtilis. Plasmids having increased numbers of copies were then selected by spreading transformed B. subtilis cells on a LB gelose medium containing a Cm concentration (25 μg/ml) which prevents the growth of cells harboring the low copy number plasmid pHT1035ΔHindIII (4+/−1 copies per chromosome equivalent).

Two plasmids having increased numbers of copies were selected for the continuation of the study (FIG. 9). Their copy numbers were determined by densitometric analysis of photographic negatives of agarose gels after electrophoresis using the parameters described by Projan et al. (1983, Determination of plasmid copy number by fluorescence densitometry. Plasmid 9: 182-190). The plasmids were designated pHT1035-15ΔHindIII and pHT1035-70ΔHindIII and have 15+/−5 and 70+/−20 copies, respectively, per chromosome equivalent. They are stable from the point of view of segregation given that 100% of the cells contained the plasmid after about 25 generations in a nonselective LB medium.

3) Construction of the shuttle vectors

It has been shown that the replication and stability regions of pHT1030 were entirely included in the 2.7 kb HpaI-BalI DNA fragment carried by pHT1035 (FIG. 9). Consequently, this DNA fragment was isolated from each of the plasmids pHT1035ΔHindIII pHT1035-15ΔHindIII and pHT1035-70ΔHindIII and used separately to construct the plasmids pHT304, pHT315 and pHT370, respectively (FIG. 10).

These plasmids may be used in the same manner as pUC19 for cloning experiments in E. coli, since the fragments were inserted at the SspI site which interrupts neither the cloning sites of the polylinker nor the bla gene. None of the polylinker site of pUC19 is duplicated.

These shuttle vectors were used to transform the B. thuringiensis strain kurstaki HD1 CryB by the electroporation procedure as described by Lereclus et al., 1989A. The recombinant clones were selected on LB gelose plates containing Er (25 μg/ml). The densitometric analysis of the total DNA preparations extracted from these clones has show that the three shuttle vectors had a copy number in B. thuringiensis similar to that of the corresponding parent plasmids in B. subtilis (FIG. 10).

B) Relationship between the delta-endotoxin production and the plasmid copy number

A 3 kb HindIII restriction fragment carrying a cryIIIA gene isolated from B. thuringiensis strain LM79 specific for the coleoptera was subcloned into the HindIII site of each of the vectors pHT304, pHT1315 and pHT370. The three resulting plasmids (pHT304ΩcryIIIA, pHT315ΩcryIIIA and pHT370ΩIIIA) carrying the cryIIIA gene in the same orientation, were introduced in the B. thuringiensis strain kurstaki HDI CryB by electroporation.

The recombinant clones were grown for 2 days at 30° C. in an HCT medium (Lecadet et al., 1980 Ber. J. Gen. Microbiol. 121: 203-212) in the presence or absence of 25 μg of Er per ml. The spore crystal preparations harvested from the cultures were examined in a phase contrast microscope and by SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis) (FIG. 11). The kurstaki HD1ΩCry-B recombinants harboring pHT304ΩcryIIIA did not produce detectable parasporal inclusions, whereas the cells harboring either pH1315ΩcryIIIA or pHT370ΩcryIIIA produced flat rhomboid crystals characteristic of strains active against coleopteran larvae (Herrnstadt et al., 1986 Bio/Techology 4: 305-308). The major components of these crystals were two polypeptides of about 73 and 67 kDa (FIG. 11). This is in agreement with earlier results which indicated that the cryIIIA gen of the tenebrionis strain of B. thuringiensis produced peptides of 73 and 67 kDa (Sekar et al., 1987). The 67 kDa component might result from proteolytic cleavage of the 73 kDa peptide. Small quantities of these peptides were found in the ssore-crystal preparations recovered from bacteria harboring pHT304ΩcryIIIA (FIG. 11, lane 2). This result shows that the production level of delta-endotoxin may be improved by increasing the copy number of the B gene, at least under the experimental conditions described here. However, there was no significant difference between the quantities of delta-endotoxin produced by the cells harboring pHT315ΩcryIIIA and those harboring pHT370Ωcry IIIA, thus indicating that above fifteen copies of plasmid per chromosome factors other than the number of copies of the cry gene limit the synthesis of the crystal proteins.

It is noted that the production of delta-endotoxins in the recombinant strains is not affected by the presence or absence at Er, suggesting that the plasmids are maintained in a stable manner in the host cells. In fact, after about 15 generations of growth followed by speculation in an HCT medium without antibiotic, all of the spores (100%) contained the plasmid.

3rd Example CONSTRUCTION OF A PLASMID CARRYING SEVERAL (2) GENES FOR DELTA-ENDOTOXINS

The plasmid pHT315ΩCRYIIIA described above is digested by the enzyme SmaI, then treated with alkaline phosphatase. The linearised plasmid is then purified on an agarose gel.

The plasmid pHT408 (Lereclus et al., 1989 FEMS 60: 211-218) is digested by the enzymes HpaI and SmaI. The 5 kb HpaI-SmaI restriction fragment carrying the cryIA(a) gene is purified on an agarose gel and ligated in the presence of DNA ligase with the plasmid pHT315ΩCRYIIIA linearised by the enzyme SmaI. The ligation mixture is used to transform E. coli. The colonies which had been grown on an LB medium containing ampicillin (100% ug/ml) are replicated on a nitrocelulose filter, then hybridized with a radioactive probe (labelled with alpha ³²P-dCTP) constituted by an internal region of the cryIa(a) gene. Only the clones transformed by the plasmid pHT315ΩcryIIIA carrying the cryIA(a) gene inserted at the SmaI site hybridize with the probe. The plasmid DNA of one of these clones is extracted and the restriction map of the plasmid is established in order to check the presence of the two genes cryIIIA and cryIA(a).

The resulting plasmid: pHT315ΩcryIIIΩcryIA(a) possesses a unique SalI restriction site which may be used to done a third DNA fragment carrying another delta-endotoxin gene and having cohesive ends with a site cut by SalI.

Such a chimeric plasmid: pHT315ΩcryIIIΩcryIA(a) or pHT315ΩcryIIIA cryIA5(a)ΩcryX, carrying a gene conferring erythromycin resistance on Gram-positive bacteria, may be used to transform B. thuringiensis and thus to construct recombinant strains expressing mutiple insecticidal activities.

14 2872 base pairs nucleic acid unknown unknown DNA (genomic) not provided misc_feature 1789..2193 /note= “ORF1 codes for 134 amino acids starting at position 2193 and terminating at position 1789.” CDS 2521..2871 promoter 75..80 promoter 98..103 1 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTAGTAATT ACTAGCATTG TCATATACAT AATAAAACGG ATATAAAAGG 360 GCGTTTTCTA TACCTAGAAG TCTTGTAAAT GTACAGGGCG TTTAGATATA GAGAACGCCC 420 TTTTTGTGTT CCGTTCCAGT GGAAGCTACC ACTTTAAAAA GATGGTCTAG TGTAGCCAAT 480 GCAGGAGAGT ACACTCGGAT ATCAGTTGTC GTTGCATTCA ACTGTCTGAC GTAAGCGAGG 540 TAAAGGACAC AAGCCTTGCA TAAAACAAGC CTACGGGATG TAAATCCTAA TAATGATGAT 600 AACCAAGACG TTAGCGGCAA AAAGTGTTGG GGGTTCAAAA TAAGACATGA TTGTGCGACT 660 GGAGTTAAAC AGTTACTCGT AAGCGGCGAT CATGACACTG ATTCACGGCT ATTCTTGTAC 720 AAGCTTTATT ACAAGGATAT GCGGGTTATA TAGCGAATCA CCCGAAAGGG AACGGTGTTG 780 GGCGTGAGAA ACGCACCGTA CGGCGCAATA CAATGCCAAT AAGCTATATA CGGACGGTAT 840 AGTAGTTTTG TAAGCTATAA CCGTTTGTCG TCAATGCAAC CAATCTCAAT TCGAGACCTC 900 GGCATCTAAG CCAGTACGAA TGAGTGGGCG TTTTAACCTC GTAAATTTTC AACAGGGGTT 960 ACTATGCCCA AAACTACATT CAGATTTCCT AACAAACTCG CCAGTATGAA AACCTTAAGA 1020 CCTTAAAGTC AAGGGATTTG AAGGATTTTA ACCTCGATTA GCAAAAAATG TAGAGTACTG 1080 AAGCAACTAC CATTAACTAA GATAGTGGGG GATTGAGGAA GAATCCAGAG CTGTTTAAAT 1140 CAAGTGAAAG ACAAGATGAA ATTAAAAGAA TAGTGAAAGA TAGGGGAGTG GTTCTCTATG 1200 AGAAAGGAAA TGGCTAGAGA ACAAAGGCAG CGGTTTATTG ATCTATTGTT AGACTTTATG 1260 GTAAAGAATC CTCATTTATT TGTTAATGGT ACAGAGGATG AAAGTAATAA TGTTGTTACA 1320 AAATGTAATA GTGATATTAA AGAGGTTGCG GAGTCATATT TAACTCTTTT ATAGTGAGAG 1380 GGTTAAAACT AATTAATATG TATTAAGGCC CAATGTTGGA ATTATTGTAT TTCACTAGGC 1440 AACCTACTTA CTAAAAGTAA GATTATCCAT TAGTGGATGT TATAATATTG GGTTTTTTAA 1500 CACAATAATC ATCGCCTTTC GGTGTCGTTT GATAGAAAAG TAACCATTAG CGATGAAAAA 1560 GTCAATATAA AAAGCCATCC GTAAAAAACG GATGGCTTAC CGTACATAGG ATCGTTGGTA 1620 GGGCGGCGTA TCCTACATCT CTGGTAACTT ACCTAGCCAA TCAAATGCTT GAGAACGGCG 1680 GTTAGATAAG CGCGTGGGGA ACCTTTCCCA CCTCAAAGAT CCTATATCAT TATTATGTTA 1740 CTTTCTACAG GTAGTATACC ATGTTCTTAT ATTTTAGTAA ACTCCCCGTT AGCTTAACAG 1800 GTCTTTGTAA GCAATTAAAC GTCCACTATT CAATCGTCTT TGGATTTTCG CAGGACCGTT 1860 TTTTAGATCG AACATAGTTG ATAAGAACAA ATAACCGCTT GGGTCCAACT TTATAGCAAT 1920 TAGTATATGG TCATTTAAAA TCTTTACCAA TTCAACGCTA TTAGGTTCTT TAGGATTTTG 1980 CCCGACATAG TCGGGGTGTT CAACGATATC TTTTATGTGC GATGAATATT TTTCATAAAT 2040 ACCAGGATGT TGTTTCTTTA CGTGCTTTAT AAATCCGGGA AACATTTTTA CATCGTTAGA 2100 AGTGCAAGTC AAGTTATATG TATCTATAAT GATTTGTGGA AGTTTTGCCA CAACAGTTGG 2160 TTTATTTACA ATCTTTTTTT TATTAGCCGT CAAATTTCTC CCTCATCTCG TCTCTTTATA 2220 TCTTTATTTT ATCATAAAGG AGTATTTGAA CCGTCGCGCG GGACAGGTTT ATGATAGGGA 2280 TATTTTATTG AATAATTGAT GGTATAAGGG ACTTTCATGC TTGGAAAGTG GGGATTATGA 2340 ATTAGATGCT TGTCCACAAT ATGTTCCAAT GTAATTAAAA TTTATGTTCC CACCTTGACC 2400 AAACATCACG TCCATACTTA AATCGTCCCT CCTTTAATAG GTAAAATATT AATTTACCTT 2460 AATAAAAAAA TAATGGATAA TAGTATTCGT CTGAATTTAT ATAATCAGGG GGAACTATTG 2520 ATG CTG GGG ATA CTA TTT ACA GCG GCG CCA TCT ACT GAT GTC GTA AAG 2568 Met Leu Gly Ile Leu Phe Thr Ala Ala Pro Ser Thr Asp Val Val Lys 1 5 10 15 GAT TTG CAA GAT AAA GTT ATA TCA TTG CAG GAT CAT GAG GTA GCG TTT 2616 Asp Leu Gln Asp Lys Val Ile Ser Leu Gln Asp His Glu Val Ala Phe 20 25 30 TTG AAC ACC ACG ATA TCT AAT ATG TTA ACA GCA GTA GGT ATT GGA GTG 2664 Leu Asn Thr Thr Ile Ser Asn Met Leu Thr Ala Val Gly Ile Gly Val 35 40 45 GCA ATT ATA ACG GCG GTT TTT ACA GCA GCG TTT GCT TAT GTT ACA TAT 2712 Ala Ile Ile Thr Ala Val Phe Thr Ala Ala Phe Ala Tyr Val Thr Tyr 50 55 60 TCT AAT AAG CGT GCT AAA AAG AAT ATG GAC GAG GCT AGT AGA AAA TTA 2760 Ser Asn Lys Arg Ala Lys Lys Asn Met Asp Glu Ala Ser Arg Lys Leu 65 70 75 80 GAA GAA GCA GAA AGT AAA GTT TCT GTG CTA GAG GAG AAA AGC GCT CAA 2808 Glu Glu Ala Glu Ser Lys Val Ser Val Leu Glu Glu Lys Ser Ala Gln 85 90 95 TTG GAG AGG AAG ATT CTT GAA GCT GAA CAA CTC TTA GCT GAT GCC AAT 2856 Leu Glu Arg Lys Ile Leu Glu Ala Glu Gln Leu Leu Ala Asp Ala Asn 100 105 110 TCT ATT TCT AAT GTG G 2872 Ser Ile Ser Asn Val 115 117 amino acids amino acid linear protein not provided 2 Met Leu Gly Ile Leu Phe Thr Ala Ala Pro Ser Thr Asp Val Val Lys 1 5 10 15 Asp Leu Gln Asp Lys Val Ile Ser Leu Gln Asp His Glu Val Ala Phe 20 25 30 Leu Asn Thr Thr Ile Ser Asn Met Leu Thr Ala Val Gly Ile Gly Val 35 40 45 Ala Ile Ile Thr Ala Val Phe Thr Ala Ala Phe Ala Tyr Val Thr Tyr 50 55 60 Ser Asn Lys Arg Ala Lys Lys Asn Met Asp Glu Ala Ser Arg Lys Leu 65 70 75 80 Glu Glu Ala Glu Ser Lys Val Ser Val Leu Glu Glu Lys Ser Ala Gln 85 90 95 Leu Glu Arg Lys Ile Leu Glu Ala Glu Gln Leu Leu Ala Asp Ala Asn 100 105 110 Ser Ile Ser Asn Val 115 134 amino acids amino acid Not Relevant unknown peptide not provided 3 Met Thr Ala Asn Lys Lys Lys Ile Val Asn Lys Pro Thr Val Val Ala 1 5 10 15 Lys Leu Pro Gln Ile Ile Ile Asp Thr Tyr Asn Leu Thr Cys Thr Ser 20 25 30 Asn Asp Val Lys Met Phe Pro Gly Phe Ile Lys His Val Lys Lys Gln 35 40 45 His Pro Gly Ile Tyr Glu Lys Tyr Ser Ser His Ile Lys Asp Ile Val 50 55 60 Glu His Pro Asp Tyr Val Gly Gln Asn Pro Lys Glu Pro Asn Ser Val 65 70 75 80 Glu Leu Val Lys Ile Leu Asn Asp His Ile Leu Ile Ala Ile Lys Leu 85 90 95 Asp Pro Ser Gly Tyr Leu Phe Leu Ser Thr Met Phe Asp Leu Lys Asn 100 105 110 Gly Pro Ala Lys Ile Gln Arg Arg Leu Asn Ser Gly Arg Leu Ile Ala 115 120 125 Tyr Lys Asp Leu Leu Ser 130 2642 base pairs nucleic acid unknown unknown DNA (genomic) not provided promoter 75..80 promoter 98..103 4 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTAGTAATT ACTAGCATTG TCATATACAT AATAAAACGG ATATAAAAGG 360 GCGTTTTCTA TACCTAGAAG TCTTGTAAAT GTACAGGGCG TTTAGATATA GAGAACGCCC 420 TTTTTGTGTT CCGTTCCAGT GGAAGCTACC ACTTTAAAAA GATGGTCTAG TGTAGCCAAT 480 GCAGGAGAGT ACACTCGGAT ATCAGTTGTC GTTGCATTCA ACTGTCTGAC GTAAGCGAGG 540 TAAAGGACAC AAGCCTTGCA TAAAACAAGC CTACGGGATG TAAATCCTAA TAATGATGAT 600 AACCAAGACG TTAGCGGCAA AAAGTGTTGG GGGTTCAAAA TAAGACATGA TTGTGCGACT 660 GGAGTTAAAC AGTTACTCGT AAGCGGCGAT CATGACACTG ATTCACGGCT ATTCTTGTAC 720 AAGCTTTATT ACAAGGATAT GCGGGTTATA TAGCGAATCA CCCGAAAGGG AACGGTGTTG 780 GGCGTGAGAA ACGCACCGTA CGGCGCAATA CAATGCCAAT AAGCTATATA CGGACGGTAT 840 AGTAGTTTTG TAAGCTATAA CCGTTTGTCG TCAATGCAAC CAATCTCAAT TCGAGACCTC 900 GGCATCTAAG CCAGTACGAA TGAGTGGGCG TTTTAACCTC GTAAATTTTC AACAGGGGTT 960 ACTATGCCCA AAACTACATT CAGATTTCCT AACAAACTCG CCAGTATGAA AACCTTAAGA 1020 CCTTAAAGTC AAGGGATTTG AAGGATTTTA ACCTCGATTA GCAAAAAATG TAGAGTACTG 1080 AAGCAACTAC CATTAACTAA GATAGTGGGG GATTGAGGAA GAATCCAGAG CTGTTTAAAT 1140 CAAGTGAAAG ACAAGATGAA ATTAAAAGAA TAGTGAAAGA TAGGGGAGTG GTTCTCTATG 1200 AGAAAGGAAA TGGCTAGAGA ACAAAGGCAG CGGTTTATTG ATCTATTGTT AGACTTTATG 1260 GTAAAGAATC CTCATTTATT TGTTAATGGT ACAGAGGATG AAAGTAATAA TGTTGTTACA 1320 AAATGTAATA GTGATATTAA AGAGGTTGCG GAGTCATATT TAACTCTTTT ATAGTGAGAG 1380 GGTTAAAACT AATTAATATG TATTAAGGCC CAATGTTGGA ATTATTGTAT TTCACTAGGC 1440 AACCTACTTA CTAAAAGTAA GATTATCCAT TAGTGGATGT TATAATATTG GGTTTTTTAA 1500 CACAATAATC ATCGCCTTTC GGTGTCGTTT GATAGAAAAG TAACCATTAG CGATGAAAAA 1560 GTCAATATAA AAAGCCATCC GTAAAAAACG GATGGCTTAC CGTACATAGG ATCGTTGGTA 1620 GGGCGGCGTA TCCTACATCT CTGGTAACTT ACCTAGCCAA TCAAATGCTT GAGAACGGCG 1680 GTTAGATAAG CGCGTGGGGA ACCTTTCCCA CCTCAAAGAT CCTATATCAT TATTATGTTA 1740 CTTTCTACAG GTAGTATACC ATGTTCTTAT ATTTTAGTAA ACTCCCCGTT AGCTTAACAG 1800 GTCTTTGTAA GCAATTAAAC GTCCACTATT CAATCGTCTT TGGATTTTCG CAGGACCGTT 1860 TTTTAGATCG AACATAGTTG ATAAGAACAA ATAACCGCTT GGGTCCAACT TTATAGCAAT 1920 TAGTATATGG TCATTTAAAA TCTTTACCAA TTCAACGCTA TTAGGTTCTT TAGGATTTTG 1980 CCCGACATAG TCGGGGTGTT CAACGATATC TTTTATGTGC GATGAATATT TTTCATAAAT 2040 ACCAGGATGT TGTTTCTTTA CGTGCTTTAT AAATCCGGGA AACATTTTTA CATCGTTAGA 2100 AGTGCAAGTC AAGTTATATG TATCTATAAT GATTTGTGGA AGTTTTGCCA CAACAGTTGG 2160 TTTATTTACA ATCTTTTTTT TATTAGCCGT CAAATTTCTC CCTCATCTCG TCTCTTTATA 2220 TCTTTATTTT ATCATAAAGG AGTATTTGAA CCGTCGCGCG GGACAGGTTT ATGATAGGGA 2280 TATTTTATTG AATAATTGAT GGTATAAGGG ACTTTCATGC TTGGAAAGTG GGGATTATGA 2340 ATTAGATGCT TGTCCACAAT ATGTTCCAAT GTAATTAAAA TTTATGTTCC CACCTTGACC 2400 AAACATCACG TCCATACTTA AATCGTCCCT CCTTTAATAG GTAAAATATT AATTTACCTT 2460 AATAAAAAAA TAATGGATAA TAGTATTCGT CTGAATTTAT ATAATCAGGG GGAACTATTG 2520 ATGCTGGGGA TACTATTTAC AGCGGCGCCA TCTACTGATG TCGTAAAGGA TTTGCAAGAT 2580 AAAGTTATAT CATTGCAGGA TCATGAGGTA GCGTTTTTGA ACACCACGAT ATCTAATATG 2640 TT 2642 1016 base pairs nucleic acid unknown unknown DNA (genomic) not provided 5 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTAGTAATT ACTAGCATTG TCATATACAT AATAAAACGG ATATAAAAGG 360 GCGTTTTCTA TACCTAGAAG TCTTGTAAAT GTACAGGGCG TTTAGATATA GAGAACGCCC 420 TTTTTGTGTT CCGTTCCAGT GGAAGCTACC ACTTTAAAAA GATGGTCTAG TGTAGCCAAT 480 GCAGGAGAGT ACACTCGGAT ATCAGTTGTC GTTGCATTCA ACTGTCTGAC GTAAGCGAGG 540 TAAAGGACAC AAGCCTTGCA TAAAACAAGC CTACGGGATG TAAATCCTAA TAATGATGAT 600 AACCAAGACG TTAGCGGCAA AAAGTGTTGG GGGTTCAAAA TAAGACATGA TTGTGCGACT 660 GGAGTTAAAC AGTTACTCGT AAGCGGCGAT CATGACACTG ATTCACGGCT ATTCTTGTAC 720 AAGCTTTATT ACAAGGATAT GCGGGTTATA TAGCGAATCA CCCGAAAGGG AACGGTGTTG 780 GGCGTGAGAA ACGCACCGTA CGGCGCAATA CAATGCCAAT AAGCTATATA CGGACGGTAT 840 AGTAGTTTTG TAAGCTATAA CCGTTTGTCG TCAATGCAAC CAATCTCAAT TCGAGACCTC 900 GGCATCTAAG CCAGTACGAA TGAGTGGGCG TTTTAACCTC GTAAATTTTC AACAGGGGTT 960 ACTATGCCCA AAACTACATT CAGATTTCCT AACAAACTCG CCAGTATGAA AACCTT 1016 1076 base pairs nucleic acid unknown unknown DNA (genomic) not provided 6 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTAGTAATT ACTAGCATTG TCATATACAT AATAAAACGG ATATAAAAGG 360 GCGTTTTCTA TACCTAGAAG TCTTGTAAAT GTACAGGGCG TTTAGATATA GAGAACGCCC 420 TTTTTGTGTT CCGTTCCAGT GGAAGCTACC ACTTTAAAAA GATGGTCTAG TGTAGCCAAT 480 GCAGGAGAGT ACACTCGGAT ATCAGTTGTC GTTGCATTCA ACTGTCTGAC GTAAGCGAGG 540 TAAAGGACAC AAGCCTTGCA TAAAACAAGC CTACGGGATG TAAATCCTAA TAATGATGAT 600 AACCAAGACG TTAGCGGCAA AAAGTGTTGG GGGTTCAAAA TAAGACATGA TTGTGCGACT 660 GGAGTTAAAC AGTTACTCGT AAGCGGCGAT CATGACACTG ATTCACGGCT ATTCTTGTAC 720 AAGCTTTATT ACAAGGATAT GCGGGTTATA TAGCGAATCA CCCGAAAGGG AACGGTGTTG 780 GGCGTGAGAA ACGCACCGTA CGGCGCAATA CAATGCCAAT AAGCTATATA CGGACGGTAT 840 AGTAGTTTTG TAAGCTATAA CCGTTTGTCG TCAATGCAAC CAATCTCAAT TCGAGACCTC 900 GGCATCTAAG CCAGTACGAA TGAGTGGGCG TTTTAACCTC GTAAATTTTC AACAGGGGTT 960 ACTATGCCCA AAACTACATT CAGATTTCCT AACAAACTCG CCAGTATGAA AACCTTAAGA 1020 CCTTAAAGTC AAGGGATTTG AAGGATTTTA ACCTCGATTA GCAAAAAATG TAGAGT 1076 705 base pairs nucleic acid unknown unknown DNA (genomic) not provided 7 CTAGTAATTA CTAGCATTGT CATATACATA ATAAAACGGA TATAAAAGGG CGTTTTCTAT 60 ACCTAGAAGT CTTGTAAATG TACAGGGCGT TTAGATATAG AGAACGCCCT TTTTGTGTTC 120 CGTTCCAGTG GAAGCTACCA CTTTAAAAAG ATGGTCTAGT GTAGCCAATG CAGGAGAGTA 180 CACTCGGATA TCAGTTGTCG TTGCATTCAA CTGTCTGACG TAAGCGAGGT AAAGGACACA 240 AGCCTTGCAT AAAACAAGCC TACGGGATGT AAATCCTAAT AATGATGATA ACCAAGACGT 300 TAGCGGCAAA AAGTGTTGGG GGTTCAAAAT AAGACATGAT TGTGCGACTG GAGTTAAACA 360 GTTACTCGTA AGCGGCGATC ATGACACTGA TTCACGGCTA TTCTTGTACA AGCTTTATTA 420 CAAGGATATG CGGGTTATAT AGCGAATCAC CCGAAAGGGA ACGGTGTTGG GCGTGAGAAA 480 CGCACCGTAC GGCGCAATAC AATGCCAATA AGCTATATAC GGACGGTATA GTAGTTTTGT 540 AAGCTATAAC CGTTTGTCGT CAATGCAACC AATCTCAATT CGAGACCTCG GCATCTAAGC 600 CAGTACGAAT GAGTGGGCGT TTTAACCTCG TAAATTTTCA ACAGGGGTTA CTATGCCCAA 660 AACTACATTC AGATTTCCTA ACAAACTCGC CAGTATGAAA ACCTT 705 70 base pairs nucleic acid unknown unknown DNA (genomic) not provided 8 AAAAGGGCGT TTTCTATACC TAGAAGTCTT GTAAATGTAC AGGGCGTTTA GATATAGAGA 60 ACGCCCTTTT 70 27 base pairs nucleic acid unknown unknown DNA (genomic) not provided 9 AGGGCGTTTA GATATAGAGA ACGCCCT 27 146 base pairs nucleic acid unknown unknown DNA (genomic) not provided 10 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCA 146 304 base pairs nucleic acid unknown unknown DNA (genomic) not provided 11 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAAT 304 314 base pairs nucleic acid unknown unknown DNA (genomic) not provided 12 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTA 314 1235 base pairs nucleic acid unknown unknown DNA (genomic) not provided 13 GCCCAATGTT GGAATTATTG TATTTCACTA GGCAACCTAC TTACTAAAAG TAAGATTATC 60 CATTAGTGGA TGTTATAATA TTGGGTTTTT TAACACAATA ATCATCGCCT TTCGGTGTCG 120 TTTGATAGAA AAGTAACCAT TAGCGATGAA AAAGTCAATA TAAAAAGCCA TCCGTAAAAA 180 ACGGATGGCT TACCGTACAT AGGATCGTTG GTAGGGCGGC GTATCCTACA TCTCTGGTAA 240 CTTACCTAGC CAATCAAATG CTTGAGAACG GCGGTTAGAT AAGCGCGTGG GGAACCTTTC 300 CCACCTCAAA GATCCTATAT CATTATTATG TTACTTTCTA CAGGTAGTAT ACCATGTTCT 360 TATATTTTAG TAAACTCCCC GTTAGCTTAA CAGGTCTTTG TAAGCAATTA AACGTCCACT 420 ATTCAATCGT CTTTGGATTT TCGCAGGACC GTTTTTTAGA TCGAACATAG TTGATAAGAA 480 CAAATAACCG CTTGGGTCCA ACTTTATAGC AATTAGTATA TGGTCATTTA AAATCTTTAC 540 CAATTCAACG CTATTAGGTT CTTTAGGATT TTGCCCGACA TAGTCGGGGT GTTCAACGAT 600 ATCTTTTATG TGCGATGAAT ATTTTTCATA AATACCAGGA TGTTGTTTCT TTACGTGCTT 660 TATAAATCCG GGAAACATTT TTACATCGTT AGAAGTGCAA GTCAAGTTAT ATGTATCTAT 720 AATGATTTGT GGAAGTTTTG CCACAACAGT TGGTTTATTT ACAATCTTTT TTTTATTAGC 780 CGTCAAATTT CTCCCTCATC TCGTCTCTTT ATATCTTTAT TTTATCATAA AGGAGTATTT 840 GAACCGTCGC GCGGGACAGG TTTATGATAG GGATATTTTA TTGAATAATT GATGGTATAA 900 GGGACTTTCA TGCTTGGAAA GTGGGGATTA TGAATTAGAT GCTTGTCCAC AATATGTTCC 960 AATGTAATTA AAATTTATGT TCCCACCTTG ACCAAACATC ACGTCCATAC TTAAATCGTC 1020 CCTCCTTTAA TAGGTAAAAT ATTAATTTAC CTTAATAAAA AAATAATGGA TAATAGTATT 1080 CGTCTGAATT TATATAATCA GGGGGAACTA TTGATGCTGG GGATACTATT TACAGCGGCG 1140 CCATCTACTG ATGTCGTAAA GGATTTGCAA GATAAAGTTA TATCATTGCA GGATCATGAG 1200 GTAGCGTTTT TGAACACCAC GATATCTAAT ATGTT 1235 2870 base pairs nucleic acid unknown unknown DNA (genomic) not provided 14 CCATCCTCCA AAGTTGGAGA GTGAGTTTTA TGTCGCAAAT ATTAATGTTT CTGGTGAACC 60 TTATCAAATT TTCGTTGATT TAATAGAAAC ATAGCGGTAA AATTAGCAGT AACTTAATAG 120 AACGGAAATG AAAAAAGCCA CTCTCATATG CTATTGGCTA CCAACCTTTA GCGAGAATGA 180 CTTAATCCTG TACAGCCATA CAGGACTTCG ACTTATAAGA GGCGCCAACC TCAAATAAGT 240 TATTTGCCTT GTTTTCGCGA ACAAGGCTTA TTAGATACAC CTATTGTACC GTTACTCTAC 300 GAATATTTCA ACTAGTAATT ACTAGCATTG TCATATACAT AATAAAACGG ATATAAAAGG 360 GCGTTTTCTA TACCTAGAAG TCTTGTAAAT GTACAGGGCG TTTAGATATA GAGAACGCCC 420 TTTTTGTGTT CCGTTCCAGT GGAAGCTACC ACTTTAAAAA GATGGTCTAG TGTAGCCAAT 480 GCAGGAGAGT ACACTCGGAT ATCAGTTGTC GTTGCATTCA ACTGTCTGAC GTAAGCGAGG 540 TAAAGGACAC AAGCCTTGCA TAAAACAAGC CTACGGGATG TAAATCCTAA TAATGATGAT 600 AACCAAGACG TTAGCGGCAA AAAGTGTTGG GGGTTCAAAA TAAGACATGA TTGTGCGACT 660 GGAGTTAAAC AGTTACTCGT AAGCGGCGAT CATGACACTG ATTCACGGCT ATTCTTGTAC 720 AAGCTTTATT ACAAGGATAT GCGGGTTATA TAGCGAATCA CCCGAAAGGG AACGGTGTTG 780 GGCGTGAGAA ACGCACCGTA CGGCGCAATA CAATGCCAAT AAGCTATATA CGGACGGTAT 840 AGTAGTTTTG TAAGCTATAA CCGTTTGTCG TCAATGCAAC CAATCTCAAT TCGAGACCTC 900 GGCATCTAAG CCAGTACGAA TGAGTGGGCG TTTTAACCTC GTAAATTTTC AACAGGGGTT 960 ACTATGCCCA AAACTACATT CAGATTTCCT AACAAACTCG CCAGTATGAA AACCTTAAGA 1020 CCTTAAAGTC AAGGGATTTG AAGGATTTTA ACCTCGATTA GCAAAAAATG TAGAGTACTG 1080 AAGCAACTAC CATTAACTAA GATAGTGGGG GATTGAGGAA GAATCCAGAG CTGTTTAAAT 1140 CAAGTGAAAG ACAAGATGAA ATTAAAAGAA TAGTGAAAGA TAGGGGAGTG GTTCTCTATG 1200 AGAAAGGAAA TGGCTAGAGA ACAAAGGCAG CGGTTTATTG ATCTATTGTT AGACTTTATG 1260 GTAAAGAATC CTCATTTATT TGTTAATGGT ACAGAGGATG AAAGTAATAA TGTTGTTACA 1320 AAATGTAATA GTGATATTAA AGAGGTTGCG GAGTCATATT TAACTCTTTT ATAGTGAGAG 1380 GGTTAAAACT AATTAATATG TATTAAGGCC CAATGTTGGA ATTATTGTAT TTCACTAGGC 1440 AACCTACTTA CTAAAAGTAA GATTATCCAT TAGTGGATGT TATAATATTG GGTTTTTTAA 1500 CACAATAATC ATCGCCTTTC GGTGTCGTTT GATAGAAAAG TAACCATTAG CGATGAAAAA 1560 GTCAATATAA AAAGCCATCC GTAAAAAACG GATGGCTTAC CGTACATAGG ATCGTTGGTA 1620 GGGCGGCGTA TCCTACATCT CTGGTAACTT ACCTAGCCAA TCAAATGCTT GAGAACGGCG 1680 GTTAGATAAG CGCGTGGGGA ACCTTTCCCA CCTCAAAGAT CCTATATCAT TATTATGTTA 1740 CTTTCTACAG GTAGTATACC ATGTTCTTAT ATTTTAGTAA ACTCCCCGTT AGCTTAACAG 1800 GTCTTTGTAA GCAATTAAAC GTCCACTATT CAATCGTCTT TGGATTTTCG CAGGACCGTT 1860 TTTTAGATCG AACATAGTTG ATAAGAACAA ATAACCGCTT GGGTCCAACT TTATAGCAAT 1920 TAGTATATGG TCATTTAAAA TCTTTACCAA TTCAACGCTA TTAGGTTCTT TAGGATTTTG 1980 CCCGACATAG TCGGGGTGTT CAACGATATC TTTTATGTGC GATGAATATT TTTCATAAAT 2040 ACCAGGATGT TGTTTCTTTA CGTGCTTTAT AAATGGGAAA CATTTTTACA TCGTTAGAAG 2100 TGCAAGTCAA GTTATATGTA TCTATAATGA TTTGTGGAAG TTTTGCCACA ACAGTTGGTT 2160 TATTTACAAT CTTTTTTTTA TTAGCCGTCA AATTTCTCCC TCATCTCGTC TCTTTATATC 2220 TTTATTTTAT CATAAAGGAG TATTTGAACC GTCGCGCGGG ACAGGTTTAT GATAGGGATA 2280 TTTTATTGAA TAATTGATGG TATAAGGGAC TTTCATGCTT GGAAAGTGGG GATTATGAAT 2340 TAGATGCTTG TCCACAATAT GTTCCAATGT AATTAAAATT TATGTTCCCA CCTTGACCAA 2400 ACATCACGTC CATACTTAAA TCGTCCCTCC TTTAATAGGT AAAATATTAA TTTACCTTAA 2460 TAAAAAAATA ATGGATAATA GTATTCGTCT GAATTTATAT AATCAGGGGG AACTATTGAT 2520 GCTGGGGATA CTATTTACAG CGGCGCCATC TACTGATGTC GTAAAGGATT TGCAAGATAA 2580 AGTTATATCA TTGCAGGATC ATGAGGTAGC GTTTTTGAAC ACCACGATAT CTAATATGTT 2640 AACAGCAGTA GGTATTGGAG TGGCAATTAT AACGGCGGTT TTTACAGCAG CGTTTGCTTA 2700 TGTTACATAT TCTAATAAGC GTGCTAAAAA GAATATGGAC GAGGCTAGTA GAAAATTAGA 2760 AGAAGCAGAA AGTAAAGTTT CTGTGCTAGA GGAGAAAAGC GCTCAATTGG AGAGGAAGAT 2820 TCTTGAAGCT GAACAACTCT TAGCTGATGC CAATTCTATT TCTAATGTGG 2870 

What is claimed is:
 1. A gram-positive bacterium transformed with a recombinant vector, wherein the vector comprises: (A) a DNA fragment that promotes, in gram-positive bacteria, replication of said recombinant vector, wherein said DNA fragment is selected from the group consisting of (1) a nucleotide sequence of SEQ ID NO:4 from Bacillus thuringiensis of about 2.6 kb and (2) a fragment included in SEQ ID NO:4, provided that said fragment allows the replication of the recombinant vector when it is under the control of a functional promoter in the gram-positive bacteria, and (B) a DNA sequence of interest operably linked to (A); wherein said vector does not comprise a fragment of the BalI—BalI fragment of SEQ ID NO:1 other than the DNA fragment of (A).
 2. The transformed gram-positive bacterium of claim 1, wherein (A) is SEQ ID NO:4.
 3. A gram-positive bacterium transformed with a recombinant vector, wherein the vector comprises (A) a DNA fragment that promotes, in gram-positive bacteria, replication of said recombinant vector, wherein said DNA fragment is selected from the group consisting of (1) the Ball-AflII fragment of SEQ ID NO:1, (2) the Ball-ScaI fragment of SEQ ID NO:1, (3) the BalI-ScaI fragment of SEQ ID NO:1 with the HindIII site deleted, (4) the Spel-AfIII fragment of SEQ ID NO:1; (5) the Ball-Nde I fragment of SEQ ID NO:1, (6) the Ball-Spe I fragment of SEQ ID NO:1, and (7) the BalI-Ssp I fragment of SEQ ID NO:1, and (B) a DNA sequence of interest operably linked to (A); wherein said vector does not comprise a fragment of the BalI—BalI fragment of SEQ ID NO:1 other than the DNA fragment of (A).
 4. The transformed gram-positive bacterium of claim 3, wherein (A) is (1).
 5. The transformed gram-positive bacterium of claim 3, wherein (A) is (2).
 6. The transformed gram-positive bacterium of claim 3, wherein (A) is (3).
 7. The transformed gram-positive bacterium of claim 3, wherein (A) is (4).
 8. The transformed gram-positive bacterium of claim 3, wherein (A) is (5).
 9. The transformed gram-positive bacterium of claim 3, wherein (A) is (6).
 10. The transformed gram-positive bacterium of claim 3, wherein (A) is (7).
 11. The transformed gram-positive bacterium of claim 1, wherein the bacterium is a Bacillus bacterium.
 12. The transformed gram-positive bacterium of claim 1, wherein the bacterium is B. thuringiensis, B. subtilis, B. sphaericus or B. megaterium.
 13. The transformed gram-positive bacterium of claim 1, wherein (B) encodes a delta-endotoxin of Bacillus thuringiensis which is toxic to insect larvae, a protease, a lipase, an amylase, a protein hormone, or an antigen of bacterial, viral or parasitic origin.
 14. The transformed gram-positive bacterium of claim 1, wherein (B) encodes cryI, cryII, cryIII or cryIV.
 15. A gram-positive bacterium transformed with a recombinant vector, wherein the vector comprises: (A) a DNA fragment that stabilizes, in gram-positive bacteria, said recombinant vector consisting of the BstUI—BstUI DNA fragment consisting of nucleotides 1692 to 2256 of SEQ ID NO:1, wherein said vector does not comprise a fragment of the BalI—BalI fragment of SEQ ID NO:1 other than the DNA fragment of (A).
 16. The transformed gram-positive bacterium of claim 15, wherein (A) consists of nucleotides 1692 to 2256 of SEQ ID NO:1.
 17. The transformed gram-positive bacterium of claim 15, wherein the host cell is a Bacillus bacteria.
 18. The transformed gram-positive bacterium of claim 15, wherein the host cell is B. thuringiensis, B. subtilis, B. sphaericus or B. megaterium.
 19. The transformed gram-positive bacterium of claim 15, wherein (B) encodes a delta-endotoxin of Bacillus thuringiensis which is toxic to insect larvae, a protease, a lipase, an amylase, a protein hormone, or an antigen of bacterial, viral or parasitic origin.
 20. The transformed gram-positive bacterium of claim 15, wherein (B) encodes cryI, cryII, cryIII or cryIV.
 21. A method of producing the transformed gram-positive bacterium of claim 1, comprising transforming a gram-positive bacterium with said recombinant vector.
 22. A method of producing the transformed gram-positive bacterium of claim 15, comprising transforming a gram-positive bacterium with said recombinant vector.
 23. An E. coli transformed with a recombinant vector, wherein the vector comprises: (A) a DNA fragment that promotes, in gram-positive bacteria, replication of said recombinant vector, wherein said DNA fragment is selected from the group consisting of (1) a nucleotide sequence of SEQ ID NO:4 from Bacillus thuringiensis of about 2.6 kb, and (2) a fragment included in SEQ ID NO:4, provided that said fragment allows the replication of the recombinant vector when it is under the control of a functional promoter in the gram-positive bacteria, and (B) a DNA sequence of interest operably linked to (A), wherein said vector does not comprise a fragment of the BalI—BalI fragment of SEQ ID NO:1 other than the DNA fragment of(A). 